Work

Identification of three novel mutations in human EYA1 protein associated with branchio-oto-renal syndrome

Year: 1998

Type: article

Study design: Observational Study

Source: Human Mutation

DOI: 10.1002/(sici)1098-1004(1998)11:6<443::aid-humu4>3.0.co;2-s

Authors: Shrawan Kumar, William J. Kimberling, Michael D. Weston, Bradley G. Schaefer, Mary Anne Berg, Henri A. M. Marres, Cor W. R. J. Cremers

Institutions: Boys Town, Boys Town National Research Hospital, University of Nebraska Medical Center, Stanford Medicine, Radboud University Nijmegen

Language: English

Topic: Head and Neck Anomalies

Subfield: Surgery

Field: Medicine

Domain: Health Sciences

SDG: Good health and well-being

Open Access status: closed

Funders: Friedreich's Ataxia Research Alliance, National Institute on Deafness and Other Communication Disorders

Award: GENTICS OF USHER SYNDROME

OpenAlex ID: W2000898022

FWCI: 4.811

Cites: 28

Cited by: 63

Related to: 10