Ravenscroft, G. Et Al. 2018. Bi-allelic mutations in MYL1 cause a severe congenital myopathy. HUMAN MOLECULAR GENETICS , vol.27, no.24 , 4263-4272.

Ravenscroft, G., Zaharieva, I. T., Bortolotti, C. A., Lambrughi, M., Pignataro, M., Borsari, M., ... Sewry, C. A.(2018). Bi-allelic mutations in MYL1 cause a severe congenital myopathy. HUMAN MOLECULAR GENETICS , vol.27, no.24, 4263-4272.

Ravenscroft, Gianina Et Al. "Bi-allelic mutations in MYL1 cause a severe congenital myopathy," HUMAN MOLECULAR GENETICS , vol.27, no.24, 4263-4272, 2018

Ravenscroft, Gianina Et Al. "Bi-allelic mutations in MYL1 cause a severe congenital myopathy." HUMAN MOLECULAR GENETICS , vol.27, no.24, pp.4263-4272, 2018

Ravenscroft, G. Et Al. (2018) . "Bi-allelic mutations in MYL1 cause a severe congenital myopathy." HUMAN MOLECULAR GENETICS , vol.27, no.24, pp.4263-4272.

@article{article, author={Gianina Ravenscroft Et Al. }, title={Bi-allelic mutations in MYL1 cause a severe congenital myopathy}, journal={HUMAN MOLECULAR GENETICS}, year=2018, pages={4263-4272} }