Ravenscroft, G. Et Al. 2013. Mutations in KLHL40 Are a Frequent Cause of Severe Autosomal-Recessive Nemaline Myopathy. AMERICAN JOURNAL OF HUMAN GENETICS , vol.93, no.1 , 6-18.

Ravenscroft, G., Miyatake, S., Lehtokari, V., Todd, E. J., Vomauen, P., Yau, K. S., ... Hayashi, Y. K.(2013). Mutations in KLHL40 Are a Frequent Cause of Severe Autosomal-Recessive Nemaline Myopathy. AMERICAN JOURNAL OF HUMAN GENETICS , vol.93, no.1, 6-18.

Ravenscroft, Gianina Et Al. "Mutations in KLHL40 Are a Frequent Cause of Severe Autosomal-Recessive Nemaline Myopathy," AMERICAN JOURNAL OF HUMAN GENETICS , vol.93, no.1, 6-18, 2013

Ravenscroft, Gianina Et Al. "Mutations in KLHL40 Are a Frequent Cause of Severe Autosomal-Recessive Nemaline Myopathy." AMERICAN JOURNAL OF HUMAN GENETICS , vol.93, no.1, pp.6-18, 2013

Ravenscroft, G. Et Al. (2013) . "Mutations in KLHL40 Are a Frequent Cause of Severe Autosomal-Recessive Nemaline Myopathy." AMERICAN JOURNAL OF HUMAN GENETICS , vol.93, no.1, pp.6-18.

@article{article, author={Gianina Ravenscroft Et Al. }, title={Mutations in KLHL40 Are a Frequent Cause of Severe Autosomal-Recessive Nemaline Myopathy}, journal={AMERICAN JOURNAL OF HUMAN GENETICS}, year=2013, pages={6-18} }