Work

DFNB79: reincarnation of a nonsyndromic deafness locus on chromosome 9q34.3

Year: 2009

Type: article

Study design: Observational Study

Source: European Journal of Human Genetics

DOI: 10.1038/ejhg.2009.121

Authors: Shahid Yar Khan, Saima Riazuddin, Mohsin Shahzad, Nazir Ahmed, Ahmad Usman Zafar, Atteeq Ur Rehman, Robert J Morell, Andrew J Griffith, Zubair M Ahmed, Sheikh Riazuddin, Thomas B Friedman

Institutions: University of the Punjab, Cincinnati Children's Hospital Medical Center, National Institutes of Health, National Institute on Deafness and Other Communication Disorders

Language: English

Topic: Hearing, Cochlea, Tinnitus, Genetics

Subfield: Sensory Systems

Field: Neuroscience

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: bronze

Funders: Ministerial Standing Committee on Scientific and Technological Cooperation of the Organization of Islamic Cooperation, National Institutes of Health, National Institute on Deafness and Other Communication Disorders

Awards: G2020362836, G334765041, G6572046415, G6870481551, Identification of Genes Causing Syndromic And Nonsyndromic Hearing Impairment, G9000213757, G9000263322, G9000312989

OpenAlex ID: W2015874019

FWCI: 0.812

Cites: 16

Cited by: 14

Related to: 10