Homozygosity Mapping Reveals Mutations of GRXCR1 as a Cause of Autosomal-Recessive Nonsyndromic Hearing Impairment
Titel:
Homozygosity Mapping Reveals Mutations of GRXCR1 as a Cause of Autosomal-Recessive Nonsyndromic Hearing Impairment
Auteur:
Schraders, Margit Lee, Kwanghyuk Oostrik, Jaap Huygen, Patrick L.M. Ali, Ghazanfar Hoefsloot, Lies H. Veltman, Joris A. Cremers, Frans P.M. Basit, Sulman Ansar, Muhammad Cremers, Cor W.R.J. Kunst, Henricus P.M. Ahmad, Wasim Admiraal, Ronald J.C. Leal, Suzanne M. Kremer, Hannie