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Published Erratum
. 2019 Sep 5;105(3):672-674.
doi: 10.1016/j.ajhg.2019.07.017.

De Novo Variants in WDR37 Are Associated with Epilepsy, Colobomas, Dysmorphism, Developmental Delay, Intellectual Disability, and Cerebellar Hypoplasia

Oguz Kanca, Jonathan C Andrews, Pei-Tseng Lee, Chirag Patel, Stephen R Braddock, Anne M Slavotinek, Julie S Cohen, Cynthia S Gubbels, Kimberly A Aldinger, Judy Williams, Maanasa Indaram, Ali Fatemi, Timothy W Yu, Pankaj B Agrawal, Gilbert Vezina, Cas Simons, Joanna Crawford, C Christopher Lau; Undiagnosed Diseases Network; Wendy K Chung, Thomas C Markello, William B Dobyns, David R Adams, William A Gahl, Michael F Wangler, Shinya Yamamoto, Hugo J Bellen, May Christine V Malicdan
Collaborators
Published Erratum

De Novo Variants in WDR37 Are Associated with Epilepsy, Colobomas, Dysmorphism, Developmental Delay, Intellectual Disability, and Cerebellar Hypoplasia

Oguz Kanca et al. Am J Hum Genet. .
No abstract available

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Figures

Figure 3
Figure 3
Conservation of WDR37 and Generation of wdr37-Null Allele (corrected)
Figure 3
Figure 3
Conservation of WDR37 and Generation of wdr37-Null Allele (original)
See this image and copyright information in PMC

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