Published in

Elsevier (Cell Press), American Journal of Human Genetics, 1(93), p. 6-18, 2013

DOI: 10.1016/j.ajhg.2013.05.004

Links

Tools

Export citation

Search in Google Scholar

Mutations in KLHL40 Are a Frequent Cause of Severe Autosomal-Recessive Nemaline Myopathy

This paper was not found in any repository, but could be made available legally by the author.
This paper was not found in any repository, but could be made available legally by the author.

Full text: Unavailable

Green circle
Preprint: archiving allowed
Orange circle
Postprint: archiving restricted
Red circle
Published version: archiving forbidden
Data provided by SHERPA/RoMEO
Beta version