GJB2 gene mutations in Slovak hearing-impaired patients of Caucasian origin: spectrum, frequencies and SNP analysis

Saved in:
Bibliographic Details
Published in:Clinical genetics 2005-12, Vol.68 (6), p.554-557
Main Authors: MINARIK, G, FERAKOVA, E, FICEK, A, POLAKOVA, H, KADASI, L
Format: Article
Language:English
Subjects:
Biological and medical sciences
Connexin 26
Connexins - genetics
DNA Primers
Ear, auditive nerve, cochleovestibular tract, facial nerve: diseases, semeiology
European Continental Ancestry Group - genetics
General aspects. Genetic counseling
Genetic Predisposition to Disease
Genetic Testing
Haplotypes - genetics
Hearing Loss - epidemiology
Hearing Loss - genetics
Humans
Medical genetics
Medical sciences
Mutation - genetics
Non tumoral diseases
Otorhinolaryngology. Stomatology
Polymorphism, Single Nucleotide - genetics
Sequence Analysis, DNA
Slovakia - epidemiology
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:
ISSN:0009-9163
1399-0004
DOI:10.1111/j.1399-0004.2005.00529.x