FIGURE SUMMARY
Title

A novel intellectual disability syndrome caused by GPI anchor deficiency due to homozygous mutations in PIGT

Authors
Kvarnung, M., Nilsson, D., Lindstrand, A., Korenke, G.C., Chiang, S.C., Blennow, E., Bergmann, M., Stödberg, T., Mäkitie, O., Anderlid, B.M., Bryceson, Y.T., Nordenskjöld, M., and Nordgren, A.
Source
Full text @ J. Med. Genet.
Fig. 4

ZFIN is incorporating published figure images and captions as part of an ongoing project. Figures from some publications have not yet been curated, or are not available for display because of copyright restrictions.

Fig. S5

ZFIN is incorporating published figure images and captions as part of an ongoing project. Figures from some publications have not yet been curated, or are not available for display because of copyright restrictions.

Acknowledgments
Full text @ J. Med. Genet.
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