Novel compound heterozygous mutations in the GPR98 (USH2C) gene identified by whole exome sequencing in a Moroccan deaf family
Crossref DOI link: https://doi.org/10.1007/s11033-017-4129-9
Published Online: 2017-09-26
Published Print: 2017-10
Update policy: https://doi.org/10.1007/springer_crossmark_policy
Bousfiha, Amale
Bakhchane, Amina
Charoute, Hicham
Detsouli, Mustapha
Rouba, Hassan
Charif, Majida
Lenaers, Guy
Barakat, Abdelhamid
License valid from 2017-09-26