Evaluation of Cx26/GJB2 in German hearing impaired persons: mutation spectrum and detection of disequilibrium between M34T (c.101T>C) and -493del10.

Human mutation

Volumn 21, Issue 1, 2003, Pages 98-

  Zoll, Barbara ^a   Petersen, Lars ^a   Lange, Katrin ^a   Gabriel, Peter ^a   Kiese Himmel, Christiane ^a   Rausch, Peter ^a   Berger, Joachim ^a   Pasche, Bastian ^a   Meins, Moritz ^a   Gross, Manfred ^a   Berger, Roswitha ^a   Kruse, Eberhard ^a   Kunz, Jürgen ^a   Sperling, Karl ^a   Laccone, Franco ^a  

^a UNIVERSITY OF GÖTTINGEN   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

CONNEXIN 26; GAP JUNCTION PROTEIN;

ARTICLE; GENE DELETION; GENE FREQUENCY; GENE LINKAGE DISEQUILIBRIUM; GENETICS; GENOTYPE; GERMANY; HEARING IMPAIRMENT; HUMAN; NUCLEOTIDE SEQUENCE; PATIENT; PHENOTYPE; POINT MUTATION;

CONNEXINS; DEAFNESS; DNA MUTATIONAL ANALYSIS; GENE FREQUENCY; GENOTYPE; GERMANY; HEARING IMPAIRED PERSONS; HUMANS; LINKAGE DISEQUILIBRIUM; PHENOTYPE; POINT MUTATION; SEQUENCE DELETION;

EID: 0037209154     PISSN: None     EISSN: 10981004     Source Type: Journal    
DOI: 10.1002/humu.9098     Document Type: Article

References (0)