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Subject genetics -- developmental -- other neurology

1. De novo variants in SUPT16H cause neurodevelopmental disorders associated with corpus callosum abnormalities. Issue 7 (10th January 2020)

Authors:
Bina, Roya; Matalon, Dena; Fregeau, Brieana; Tarsitano, Jacqueline Joani; Aukrust, Ingvild; Houge, Gunnar; Bend, Renee; Warren, Hannah; Stevenson, Roger E; Stuurman, Kyra Eva; Barkovich, A James; Sherr, Elliott H.
Journal:
Journal of medical genetics
Issue:
Volume 57:Issue 7(2020)
Page Start:
461
Record Type:
Journal Article
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