Gene: MPZ ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4359
Gene Symbol: MPZ
MPZ 		0.020 GeneticVariation disease BEFREE The breakpoint is situated between two hearing impairment (HI) loci, DFNA49 and DFNA7, and in close proximity to the MPZ gene previously shown to be involved in autosomal dominant Charcot-Marie-Tooth syndrome (CMT1B) with auditory neuropathy. 17765268 2008
Entrez Id: 4359
Gene Symbol: MPZ
MPZ 		0.020 GeneticVariation disease BEFREE Pathology and physiology of auditory neuropathy with a novel mutation in the MPZ gene (Tyr145->Ser). 12805115 2003