A novel founder MYO15A frameshift duplication is the major cause of genetic hearing loss in Oman
Academic Article
Publication Date:
2017
Short description:
A novel founder MYO15A frameshift duplication is the major cause of genetic hearing loss in Oman / Palombo, F., Al Wardy, N., Ruscone, G.A.G., Oppo, M., Kindi, M.N.A., Angius, A., Al Lamki, K., Girotto, G., Giangregorio, T., Benelli, M., Magi, A., Seri, M., Gasparini, P., Cucca, F., Sazzini, M., Al Khabori, M., Pippucci, T., Romeo, G.. - In: JOURNAL OF HUMAN GENETICS. - ISSN 1435-232X. - 62:2(2017), pp. 259-264. [10.1038/jhg.2016.120]
Iris type:
1.1 Articolo in rivista
List of contributors:
Palombo, F; Al Wardy, N; Ruscone, G. A. G; Oppo, Manuela; Kindi, M. N. A; Angius, Andrea; Al Lamki, K; Girotto, G; Giangregorio, T; Benelli, M; Magi, A; Seri, M; Gasparini, P; Cucca, Francesco; Sazzini, M; Al Khabori, M; Pippucci, T; Romeo, G.
Published in: