Disorders


 

DFNB49 Nonsyndromic Hearing Loss and Deafness


Synonym(s): DFNB 49 Nonsyndromic Hearing Loss and Deafness

 

OMIM

GeneLocusProtein
MARVELD25q13.1MARVEL domain-containing protein 2

Laboratory Test Method Prenatal Carrier *
2nd School of Medicine Charles University - Department of Child Neurology, DNA Laboratory - Praha 5, Czech Republic• Sequence analysis of select exons
  
Center for Human Genetics, Bioscientia GmbH - Ingelheim, Germany  

* 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.

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