通过全外显子组测序在患有埃默里-德雷弗斯肌营养不良症的双胞胎中鉴定出一种新的EMD突变。

Case Reports in Genetics Pub Date : 2020-08-24 eCollection Date: 2020-01-01 DOI:10.1155/2020/2071738
Xiafei Dai, Rong Luo, Yang Chen, Chenqing Zheng, Yibin Tang, Hongmei Zhang, Ye Su, Tao He, Xiaoping Li
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引用次数: 1

摘要

本病例报告了一种新的半合子移码EMD突变(c.487delA, p.Ser163fs),发生在患有严重心脏受累和轻度肌肉无力的埃莫里-德莱弗斯肌营养不良家族的双胞胎中。它们的母亲携带了同样的杂合突变。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A Novel <i>EMD</i> Mutation Identified by Whole-Exome Sequencing in Twins with Emery-Dreifuss Muscular Dystrophy.

A Novel <i>EMD</i> Mutation Identified by Whole-Exome Sequencing in Twins with Emery-Dreifuss Muscular Dystrophy.

A Novel <i>EMD</i> Mutation Identified by Whole-Exome Sequencing in Twins with Emery-Dreifuss Muscular Dystrophy.

A Novel EMD Mutation Identified by Whole-Exome Sequencing in Twins with Emery-Dreifuss Muscular Dystrophy.

This case reports a novel hemizygous frameshift EMD mutation (c.487delA, p.Ser163fs) in twins of an Emery-Dreifuss muscular dystrophy family with severe cardiac involvement and mild muscle weakness. Their mother carried the same heterozygous mutation.

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