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Homozygosity mapping reveals mutations of GRXCR1 as a cause of autosomal-recessive nonsyndromic hearing impairment

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Description scientific article
Author/s

author: Margit Schraders  Patrick L M Huygen  Sulman Basit  Wasim Ahmad  Joris A Veltman  Kwanghyuk Lee  Frans P M Cremers  Hannie Kremer  Henricus Kunst  Suzanne M. Leal  Cor W. R. J. Cremers  Lies H. Hoefsloot  Jaap Oostrik  Ronald J Admiraal 

Publication date February 4, 2010
Language English
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