Author:
Lenherr Nina,Christodoulou John,Duley John,Dobritzsch Doreen,Fairbanks Lynette,Datta Alexandre N.,Filges Isabel,Gürtler Nicolas,Roelofsen Jeroen,van Kuilenburg André B.P.,Kemper Claudia,West Erin E.,Szinnai Gabor,Huemer Martina
Funder
State Government of Victoria
Subject
Endocrinology,Genetics,Molecular Biology
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4. X-linked Charcot-Marie-Tooth disease, Arts syndrome, and prelingual non-syndromic deafness form a disease continuum: evidence from a family with a novel PRPS1 mutation;Synofzik;Orphanet J Rare Dis.,2014
5. Hearing loss and PRPS1 mutations: wide spectrum of phenotypes and potential therapy;Liu;Int. J. Audiol.,2013
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