Disorders

DFNB59 Nonsyndromic Hearing Loss and Deafness

Synonym(s): DFNB 59 Nonsyndromic Hearing Loss and Deafness

Gene	Locus	Protein
DFNB59	2q31.2

Laboratory	Test Method	Prenatal	Carrier *
Center for Human Genetics, Bioscientia GmbH - Ingelheim, Germany
GENETAQ, Molecular Genetics Centre - Malaga, Spain
Harvard Medical School and Partners Healthcare, Laboratory for Molecular Medicine - Cambridge, MA, USA
Radboud University Nijmegen Medical Centre, Genome Diagnostics Nijmegen - Nijmegen, Netherlands

^* Carrier column is relevant to autosomal recessive and X-linked inheritance; column will be blank when it is not relevant (e.g. autosomal dominant inheritance, microdeletions/duplications) and/or is not offered by the lab.