一名由MED12新变异引起的Maat - Kievit - Brunner表型X连锁Ohdo综合征女性患者

Hiroaki Murakami, Yumi Enomoto, Y. Tsurusaki, Y. Sugio, K. Kurosawa
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引用次数: 18

摘要

MED12是大型多蛋白介质复合物的一个组成部分。MED12变异与三种不同的x连锁智力残疾(ID)综合征有关,包括Maat-Kievit-Brunner表型的Ohdo综合征(OSMKB)、Opitz-Kaveggia综合征(FG)和Lujan-Fryns综合征(LFS)。这篇文章受版权保护。版权所有。
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A female patient with X‐linked Ohdo syndrome of the Maat‐Kievit‐Brunner phenotype caused by a novel variant of MED12
MED12 is a component of the large multiprotein Mediator complex. MED12 variants have been linked to three different X-linked intellectual disability (ID) syndromes, including Ohdo syndrome of the Maat-Kievit-Brunner phenotype (OSMKB), Opitz-Kaveggia (FG) syndrome, and Lujan-Fryns syndrome (LFS). This article is protected by copyright. All rights reserved.
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