Nemaline Rod/Cap Myopathy Due to Novel Homozygous MYPN Mutations: The First Report from South Asia and Comprehensive Literature Review.
J Clin Neurol
; 17(3): 409-418, 2021 Jul.
Article
in En
| MEDLINE
| ID: mdl-34184449
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1
Collection:
01-internacional
Database:
MEDLINE
Type of study:
Systematic_reviews
Language:
En
Journal:
J Clin Neurol
Year:
2021
Document type:
Article
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