FIGURE SUMMARY
Title

Bi-allelic premature truncating variants in LTBP1 cause cutis laxa syndrome

Authors
Pottie, L., Adamo, C.S., Beyens, A., Lütke, S., Tapaneeyaphan, P., De Clercq, A., Salmon, P.L., De Rycke, R., Gezdirici, A., Gulec, E.Y., Khan, N., Urquhart, J.E., Newman, W.G., Metcalfe, K., Efthymiou, S., Maroofian, R., Anwar, N., Maqbool, S., Rahman, F., Altweijri, I., Alsaleh, M., Abdullah, S.M., Al-Owain, M., Hashem, M., Houlden, H., Alkuraya, F.S., Sips, P., Sengle, G., Callewaert, B.
Source
Full text @ Am. J. Hum. Genet.
Fig. 6

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. 7

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 @ Am. J. Hum. Genet.
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