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Article

Novel deletion in the ACTA1 gene associated with milder phenotype of nemaline myopathy in Chinese patient: a case report.

Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology - 1 Dec 2021

Yang Li, Mu Xin, Shen Qiuyan, Zhang Dan, Xu Yanming

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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PMID: 34596777
DOI: 10.1007/s10072-021-05625-0

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

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Novel deletion in the ACTA1 gene associated with milder phenotype of nemaline myopathy in Chinese patient: a case report.PMID 34596777Read ↗

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