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

Authors :
Dan Zhang
Li Yang
Xin Mu
Qiuyan Shen
Yanming Xu
Source :
Neurological Sciences. 42:5401-5405
Publication Year :
2021
Publisher :
Springer Science and Business Media LLC, 2021.

Subjects

Subjects :
medicine.medical_specialty
Neurology
business.industry
Dermatology
General Medicine
medicine.disease
Bioinformatics
Phenotype
Psychiatry and Mental health
Nemaline myopathy
medicine
Neurology (clinical)
Neurosurgery
business
Gene
Neuroradiology

Details

ISSN :
15903478 and 15901874
Volume :
42
Database :
OpenAIRE
Journal :
Neurological Sciences
Accession number :
edsair.doi...........68b5a82b20a4e0caff5fa6ea4c845eef

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