Výsledky vyhledávání - "Anja Volz-Peters"

Identification of a novel mutation in WFS1 in a family affected by low-frequency hearing impairment

Autor: R. Berger, Anja Volz-Peters, Peter Rausch, Jürgen Kunz, Steffen Uebe, Ben Marquez-Klaka

Publikováno v: Mutation research. 525(1-2)

Previously we confirmed linkage of autosomal dominantly inherited low-frequency sensorineural hearing impairment (LFSNHI) in a German family to the genetic locus DFNA6/DFNA14 on chromosome 4p16.3 close to the markers D4S432 and D4S431. Analysis of da

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e7ca932cf0d11ac62f532b6c05794e59
https://pubmed.ncbi.nlm.nih.gov/12650912

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