Work

Novel variant p.E269K confirms causative role of PLS1 mutations in autosomal dominant hearing loss

Year: 2019

Type: article

Source: Clinical Genetics

DOI: 10.1111/cge.13626

Authors: Oscar Diaz‐Horta, Guney Bademci, Suna Tokgoz‐Yilmaz, Shengru Guo, Faraz Zafeer, Claire J. Sineni, Duygu Duman, Amjad Farooq, Mustafa Tekin

Institutions: University of Miami, Ankara University, Dr. John T. Macdonald Foundation

Language: English

Topic: Hearing, Cochlea, Tinnitus, Genetics

Subfield: Sensory Systems

Field: Neuroscience

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

Funder: National Institute on Deafness and Other Communication Disorders

Awards: G2596499796, G8599100277

OpenAlex ID: W2969658451

FWCI: 0.514

Cites: 19

Cited by: 14

Related to: 10