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

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Published in Hum Mutat on January 01, 1998

Authors

S Kumar1, W J Kimberling, M D Weston, B G Schaefer, M A Berg, H A Marres, C W Cremers

Author Affiliations

1: Department of Genetics, Center for Hereditary and Communication Disorders, Boys Town National Research Hospital, Omaha, Nebraska 68131, USA. Kumar@boystown.org

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