Work

Limb girdle muscular dystrophy D3 HNRNPDL related in a Chinese family with distal muscle weakness caused by a mutation in the prion-like domain

Year: 2019

Type: article

Source: Journal of Neurology

DOI: 10.1007/s00415-018-9165-4

Authors: Yanan Sun, Hai Chen, Yan Lu, Jianying Duo, Lin Lei, Yasheng OuYang, Yifeng Hao, Yuwei Da, Xin-Ming Shen

Institutions: Capital Medical University, Xuan Wu Hospital of the Capital Medical University, Mayo Clinic

Language: English

Topic: Muscle Physiology and Disorders

Subfield: Molecular Biology

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

Funder: National Key Research and Development Program of China

OpenAlex ID: W2906859860

FWCI: 1.218

Cites: 33

Cited by: 42

Related to: 10