Dysferlinopathy in a cohort of Chinese patients: clinical features, mutation spectrum, and imaging findings
Chin Med J (Engl)
.
2021 Feb 8;134(5):622-624.
doi: 10.1097/CM9.0000000000001343.
Authors
Qi-Fu Guo
1
,
Zhi-Xian Ye
1
,
Liang-Liang Qiu
1
,
Xin Lin
1
,
Jia-He Lai
1
,
Min-Ting Lin
1
,
Zhi-Qiang Wang
1
2
,
Ning Wang
1
2
,
Feng Lin
1
Affiliations
1
Department of Neurology and Institute of Neurology, The First Affiliated Hospital of Fujian Medical University, Fuzhou, Fujian 350005, China.
2
Fujian Key Laboratory of Molecular Neurology, Fuzhou, Fujian 350005, China.
PMID:
33560664
PMCID:
PMC7929533
DOI:
10.1097/CM9.0000000000001343
No abstract available
MeSH terms
China
Dysferlin / genetics
Humans
Muscular Dystrophies, Limb-Girdle* / diagnostic imaging
Muscular Dystrophies, Limb-Girdle* / genetics
Mutation
Substances
Dysferlin
Supplementary concepts
Dysferlinopathy