Novel MYO15A variants are associated with hearing loss in the two Iranian pedigrees

Authors: Somayeh Khatami, Masomeh Askari, Fatemeh Bahreini, Morteza Hashemzadeh-Chaleshtori, Saeed Hematian, Samira Asgharzade

Source: BMC Medical Genetics, Vol 21, Iss 1, Pp 1-7 (2020)

Subject Terms: MYO15A, Whole exome sequencing, First approach, Consanguineous, Internal medicine, RC31-1245, Genetics, QH426-470

File Description: electronic resource

Relation: http://link.springer.com/article/10.1186/s12881-020-01168-x; https://doaj.org/toc/1471-2350

Access URL: https://doaj.org/article/2c82a74a1b6e4c9198ce2666679245ff