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Literature DB >> 17035706

Inclusion body myopathy-like changes in a family with cerebellar atrophy, mental retardation and abnormal pupils.

S Gambelli, M T Dotti, A Malandrini, G Berti, G Serni, A Federico.

Abstract

Entities: Disease

Mesh：

Year: 2006 PMID： 17035706 DOI： 10.1159/000096182

Source DB: PubMed Journal: Eur Neurol ISSN： 0014-3022 Impact factor: 1.710

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1. Oculopharyngeal Weakness, Hypophrenia, Deafness, and Impaired Vision: A Novel Autosomal Dominant Myopathy with Rimmed Vacuoles.

Authors: Ting Chen; Xiang-Hui Lu; Hui-Fang Wang; Rui Ban; Hua-Xu Liu; Qiang Shi; Qian Wang; Xi Yin; Chuan-Qiang Pu
Journal: Chin Med J (Engl) Date: 2016-08-05 Impact factor: 2.628

1 in total