Disruption of PHF21A causes syndromic intellectual disability with craniofacial anomalies, epilepsy, hypotonia, and neurobehavioral problems including autism

Disruption of PHF21A causes syndromic intellectual disability with craniofacial anomalies, epilepsy, hypotonia, and neurobehavioral problems including autism

Abstract Background PHF21A has been associated with intellectual disability and craniofacial anomalies based on its deletion in the Potocki-Shaffer syndrome region at 11p11.2 and its disruption in three patients with balanced translocations. In addition, three patients with de novo truncating mutati...

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Main Authors: Hyung‐Goo Kim, Jill A. Rosenfeld, Daryl A. Scott, Gerard Bénédicte, Jonathan D. J. Labonne, Jason Brown, Marianne McGuire, Sonal Mahida, Sakkubai Naidu, Jacqueline Gutierrez, Gaëtan Lesca, Vincent des Portes, Ange-Line Bruel, Arthur Sorlin, Fan Xia, Yline Capri, Eric Muller, Dianalee McKnight, Erin Torti, Franz Rüschendorf, Oliver Hummel, Zeyaul Islam, Prasanna R. Kolatkar, Lawrence C. Layman, Duchwan Ryu, Il‐Keun Kong, Suneeta Madan‐Khetarpal, Cheol‐Hee Kim
Format: Artigo
Jezik:angleščina
Izdano: 2019
Online dostop:https://doi.org/10.1186/s13229-019-0286-0
https://molecularautism.biomedcentral.com/track/pdf/10.1186/s13229-019-0286-0
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https://doi.org/10.1186/s13229-019-0286-0
https://molecularautism.biomedcentral.com/track/pdf/10.1186/s13229-019-0286-0

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