A novel autosomal dominant inclusion body myopathy linked to 7q22.1-31.1.

A novel autosomal dominant inclusion body myopathy linked to 7q22.1-31.1.

We describe a novel autosomal dominant hereditary inclusion body myopathy (HIBM) that clinically mimics limb girdle muscular dystrophy in a Chinese family. We performed a detailed clinical assessment of 36 individuals spanning four generations. The age of onset ranged from the 30s to the 50s. Hip gi...

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Bibliographic Details
Main Authors: Yan Lu, Xingang Li, Min Wang, Xin Li, Feng Zhang, Yun Li, Meng Zhang, Yuwei Da, Jun Yu, Jianping Jia
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3377676?pdf=render

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http://europepmc.org/articles/PMC3377676?pdf=render

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