A novel nonsense mutation in MYO15A is associated with non-syndromic hearing loss: a case report

• Main Authors: Di Ma (Author), Shanshan Shen (Author), Hui Gao (Author), Hui Guo (Author), Yumei Lin (Author), Yuhua Hu (Author), Ruanzhang Zhang (Author), Shayan Wang (Author)
• Format: Book
• Published: BMC, 2018-08-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

Abstract Background Hearing loss is genetically heterogeneous and is one of the most common human defects. Here we screened the underlying mutations that caused autosomal recessive non-syndromic hearing loss in a Chinese family. Case presentation The proband with profound hearing loss had received a...