A genotype-phenotype correlation with gender-effect for hearing impairment caused by TECTA mutations

Cellular Physiology and Biochemistry

Volumn 14, Issue 4-6, 2004, Pages 369-376

  Pfister, Markus ^a   Thiele, Holger ^b,c   Van Camp, Guy ^d   Fransen, Erik ^d   Apaydin, Fazil ^e   Aydin, Ömer ^f   Leistenschneider, Peter ^a   Devoto, Marcella ^g,h   Zenner, Hans Peter ^a   Blin, Nikolaus ^a   Nürnberg, Peter ^b,c   Ozkarakas, Haluk ^f   Kupka, Susan ^a  

^a UNIVERSITY OF TÜBINGEN   (Germany)

^b MAX DELBRÜCK CENTER FOR MOLECULAR MEDICINE   (Germany)

^c HUMBOLDT UNIVERSITY   (Germany)

^d UNIVERSITY OF ANTWERP   (Belgium)

^e EGE UNIVERSITY   (Turkey)

^f KOCAELI UNIVERSITY   (Turkey)

^g NEMOURS ALFRED I DUPONT HOSPITAL FOR CHILDREN   (United States)

^h UNIVERSITY OF GENOA   (Italy)

Author keywords

Alpha tectorin; Gender effect; Genotype phenotype correlation; Hearing impairment; TECTA

Indexed keywords

CYSTEINE; GLYCINE;

AMINO ACID SUBSTITUTION; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CHROMOSOME; CLINICAL ARTICLE; COCHLEA DUCT; CODON; DISEASE MARKER; DISULFIDE BOND; EXON; FAMILY; FEMALE; GENE; GENE MUTATION; GENE SEQUENCE; GENOTYPE PHENOTYPE CORRELATION; HEARING IMPAIRMENT; HUMAN; LINKAGE ANALYSIS; MALE; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; PROTEIN PROTEIN INTERACTION; TECTA GENE; TURKEY (REPUBLIC);

EID: 4444237227     PISSN: 10158987     EISSN: None     Source Type: Journal    
DOI: 10.1159/000080347     Document Type: Article

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