DOI:
10.1055/s-00000041
Neuropediatrics
LinksClose Window
References
Ravenscroft G, Miyatake S, Lehtokari V-L. , et al.
Mutations in KLHL40 are a frequent cause of severe autosomal-recessive nemaline myopathy.
Am J Hum Genet 2013;
93 (01) 6-18
We do not assume any responsibility for the contents of the web pages of other providers.