Congenital myopathy with selective muscle atrophy, necklace-like fibres/central cores and craniosynostosis associated with recessive mutations in SCN4A.
Year: 2016
Type: conference-paper
Authors: El-Murshed, M, Gonorazy, H, Marshall, CR, Hazrati, L-N, Mannikko, R, Ray, PN, Yoon, G
Language: English
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: closed
OpenAlex ID: W7055291950