EMQN Best Practice guidelines for diagnostic testing of mutations causing non-syndromic hearing impairment at the DFNB1 locus.

Authors :: Hoefsloot LH
Roux AF
Bitner-Glindzicz M
Source :: European journal of human genetics : EJHG [Eur J Hum Genet] 2013 Nov; Vol. 21 (11), pp. 1325-9. Date of Electronic Publication: 2013 May 22.
Publication Year :: 2013

Subjects :: Connexin 26
Connexin 30
Deafness genetics
Europe
Genetic Testing
Humans
Mutation, Missense genetics
Phenotype
Sequence Deletion genetics
Connexins genetics
Genetic Loci genetics
Molecular Biology
Molecular Diagnostic Techniques
Mutation genetics
Practice Guidelines as Topic

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