Clinical and genetic characteristics of Chinese patients with reducing body myopathy-Reference-Cited by-同舟云学术

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Clinical and genetic characteristics of Chinese patients with reducing body myopathy

Published:2021-05 Issue:5 Volume:31 Page:442-449
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Chen Lei,Lin Hui-Xia,Yang Xin-Xia,Chen Dian-Fu,Dong Hai-Lin,Yu Hao,Liu Gong-Lu,Wu Zhi-Ying

Funder

Natural Science Foundation of Zhejiang Province

Zhejiang University

Publisher

Elsevier BV

Subject

Genetics (clinical),Neurology (clinical),Neurology,Pediatrics, Perinatology and Child Health

Reference30 articles.

1. Chromosomal mapping, tissue distribution and cDNA sequence of four-and-a-half LIM domain protein 1 (FHL1);Lee;Gene,1998

2. The LIM domain: from the cytoskeleton to the nucleus;Kadrmas;Nat Rev Mol Cell Biol,2004

3. Characterization of tissue-specific LIM domain protein (FHL1C) which is an alternatively spliced isoform of a human LIM-only protein (FHL1);Ng;J Cell Biochem,2001

4. Characterization of a brain-specific nuclear LIM domain protein (FHL1B) which is an alternatively spliced variant of FHL1;Lee;Gene,1999

5. Characterization of Two Isoforms of the Skeletal Muscle LIM Protein 1, SLIM1

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