PUBLICATION
CORRECTION: Biallelic variants in HPDL cause pure and complicated hereditary spastic paraplegia
- Authors
- Wiessner, M., Maroofian, R., Ni, M.Y., Pedroni, A., Müller, J.S., Stucka, R., Beetz, C., Efthymiou, S., Santorelli, F.M., Alfares, A.A., Zhu, C., Uhrova Meszarosova, A., Alehabib, E., Bakhtiari, S., Janecke, A.R., Otero, M.G., Chen, J.Y.H., Peterson, J.T., Strom, T.M., De Jonghe, P., Deconinck, T., De Ridder, W., De Winter, J., Pasquariello, R., Ricca, I., Alfadhel, M., van de Warrenburg, B.P., Portier, R., Bergmann, C., Ghasemi Firouzabadi, S., Jin, S.C., Bilguvar, K., Hamed, S., Abdelhameed, M., Haridy, N.A., Maqbool, S., Rahman, F., Anwar, N., Carmichael, J., Pagnamenta, A.T., Wood, N.W., Tran Mau-Them, F., Haack, T., Genomics England Research Consortium, PREPARE network, Di Rocco, M., Ceccherini, I., Iacomino, M., Zara, F., Salpietro, V., Scala, M., Rusmini, M., Xu, Y., Wang, Y., Suzuki, Y., Koh, K., Nan, H., Ishiura, H., Tsuji, S., Lambert, L., Schmitt, E., Lacaze, E., Küpper, H., Dredge, D., Skraban, C., Goldstein, A., Willis, M.J.H., Grand, K., Graham, J.M., Lewis, R.A., Millan, F., Duman, Ö., Olgac Dundar, N., Uyanik, G., Schöls, L., Nürnberg, P., Nürnberg, G., Català-Bordes, A., Seeman, P., Kuchar, M., Darvish, H., Rebelo, A., Bouçanova, F., Medard, J.J., Chrast, R., Auer-Grumbach, M., Alkuraya, F.S., Shamseldin, H., Al Tala, S., Rezazadeh Varaghchi, J., Najafi, M., Deschner, S., Gläser, D., Hüttel, W., Kruer, M.C., Kamsteeg, E.J., Takiyama, Y., Züchner, S., Baets, J., Synofzik, M., Schüle, R., Horvath, R., Houlden, H., Bartesaghi, L., Lee, H.J., Ampatzis, K., Pierson, T.M., Senderek, J.
- ID
- ZDB-PUB-220906-261
- Date
- 2021
- Source
- Brain : a journal of neurology 144: e70 (Other)
- Registered Authors
- Keywords
- none
- MeSH Terms
- none
- PubMed
- 34480796 Full text @ Brain
Citation
Wiessner, M., Maroofian, R., Ni, M.Y., Pedroni, A., Müller, J.S., Stucka, R., Beetz, C., Efthymiou, S., Santorelli, F.M., Alfares, A.A., Zhu, C., Uhrova Meszarosova, A., Alehabib, E., Bakhtiari, S., Janecke, A.R., Otero, M.G., Chen, J.Y.H., Peterson, J.T., Strom, T.M., De Jonghe, P., Deconinck, T., De Ridder, W., De Winter, J., Pasquariello, R., Ricca, I., Alfadhel, M., van de Warrenburg, B.P., Portier, R., Bergmann, C., Ghasemi Firouzabadi, S., Jin, S.C., Bilguvar, K., Hamed, S., Abdelhameed, M., Haridy, N.A., Maqbool, S., Rahman, F., Anwar, N., Carmichael, J., Pagnamenta, A.T., Wood, N.W., Tran Mau-Them, F., Haack, T., Genomics England Research Consortium, PREPARE network, Di Rocco, M., Ceccherini, I., Iacomino, M., Zara, F., Salpietro, V., Scala, M., Rusmini, M., Xu, Y., Wang, Y., Suzuki, Y., Koh, K., Nan, H., Ishiura, H., Tsuji, S., Lambert, L., Schmitt, E., Lacaze, E., Küpper, H., Dredge, D., Skraban, C., Goldstein, A., Willis, M.J.H., Grand, K., Graham, J.M., Lewis, R.A., Millan, F., Duman, Ö., Olgac Dundar, N., Uyanik, G., Schöls, L., Nürnberg, P., Nürnberg, G., Català-Bordes, A., Seeman, P., Kuchar, M., Darvish, H., Rebelo, A., Bouçanova, F., Medard, J.J., Chrast, R., Auer-Grumbach, M., Alkuraya, F.S., Shamseldin, H., Al Tala, S., Rezazadeh Varaghchi, J., Najafi, M., Deschner, S., Gläser, D., Hüttel, W., Kruer, M.C., Kamsteeg, E.J., Takiyama, Y., Züchner, S., Baets, J., Synofzik, M., Schüle, R., Horvath, R., Houlden, H., Bartesaghi, L., Lee, H.J., Ampatzis, K., Pierson, T.M., Senderek, J. (2021) CORRECTION: Biallelic variants in HPDL cause pure and complicated hereditary spastic paraplegia. Brain : a journal of neurology. 144:e70.
Abstract
Manuela Wiessner, Reza Maroofian, Meng-Yuan Ni, Andrea Pedroni, Juliane S. Müller, Rolf Stucka, Christian Beetz, Stephanie Efthymiou, Filippo M. Santorelli, Ahmed A. Alfares, Changlian Zhu, Anna Uhrova Meszarosova, Elham Alehabib, Somayeh Bakhtiari, Andreas R. Janecke, Maria Gabriela Otero, Jin Yun Helen Chen, James T. Peterson, Tim M. Strom, Peter De Jonghe, Tine Deconinck, Willem De Ridder, Jonathan De Winter, Rossella Pasquariello, Ivana Ricca, Majid Alfadhel, Bart P. van de Warrenburg, Ruben Portier, Carsten Bergmann, Saghar Ghasemi Firouzabadi, Sheng Chih Jin, Kaya Bilguvar, Sherifa Hamed, Mohammed Abdelhameed, Nourelhoda A. Haridy, Shazia Maqbool, Fatima Rahman, Najwa Anwar, Jenny Carmichael, Alistair T. Pagnamenta, Nick W. Wood, Frederic Tran Mau-Them, Tobias Haack, Genomics England Research Consortium, PREPARE network, Maja Di Rocco, Isabella Ceccherini, Michele Iacomino, Federico Zara, Vincenzo Salpietro, Marcello Scala, Marta Rusmini, Yiran Xu, Yinghong Wang, Yasuhiro Suzuki, Kishin Koh, Haitian Nan, Hiroyuki Ishiura, Shoji Tsuji, Laëtitia Lambert, Emmanuelle Schmitt, Elodie Lacaze, Hanna Küpper, David Dredge, Cara Skraban, Amy Goldstein, Mary J. H. Willis, Katheryn Grand, John M. Graham Jr, Richard A. Lewis, Francisca Millan, Özgür Duman, Nihal Olgac Dundar, Gökhan Uyanik, Ludger Schöls, Peter Nürnberg, Gudrun Nürnberg, Andrea Català-Bordes, Pavel Seeman, Martin Kuchar, Hossein Darvish, Adriana Rebelo, Filipa Bouçanova, Jean-Jacques Medard, Roman Chrast, Michaela Auer-Grumbach, Fowzan S. Alkuraya, Hanan Shamseldin, Saeed Al Tala, Jamileh Rezazadeh Varaghchi, Maryam Najafi, Selina Deschner, Dieter Gläser, Wolfgang Hüttel, Michael C. Kruer, Erik-Jan Kamsteeg, Yoshihisa Takiyama, Stephan Züchner, Jonathan Baets, Matthis Synofzik, Rebecca Schüle, Rita Horvath, Henry Houlden, Luca Bartesaghi, Hwei-Jen Lee, Konstantinos Ampatzis, Tyler Mark Pierson and Jan Senderek. Biallelic variants in HPDL cause pure and complicated hereditary spastic paraplegia. Brain 2021;144(5):1422?1434. doi:10.1093/brain/awab041
The publisher apologizes for publishing an incorrect version of the article. This has been corrected.
Errata / Notes
This article corrects ZDB-PUB-210511-10 .
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping