Re-assigning the DFNB33 locus to chromosome 10p11.23-q21.1

European Journal of Human Genetics

Volumn 17, Issue 1, 2009, Pages 122-124

  Belguith, Hanen ^a,b   Masmoudi, Saber ^b   Medlej Hashim, Myrna ^a   Chouery, Eliane ^a   Weil, Dominique ^c   Ayadi, Hammadi ^b   Petit, Christine ^c   Mégarbané, André ^a  

^a SAINT JOSEPH UNIVERSITY   (Lebanon)

^b CENTRE DE BIOTECHNOLOGIE DE SFAX   (Tunisia)

^c INSTITUT PASTEUR   (France)

Author keywords

[No Author keywords available]

Indexed keywords

CONNEXIN 40; CONNEXIN 40.1; GENE PRODUCT; PROTEIN DFNB33; PROTEIN FXYD4; REGULATOR PROTEIN; UNCLASSIFIED DRUG;

ARTICLE; ASIAN; AUTOSOMAL RECESSIVE DISORDER; CASE REPORT; CHROMOSOME 10P; CHROMOSOME 9Q; CHROMOSOME ANALYSIS; CONSANGUINITY; FEMALE; GENE IDENTIFICATION; GENE LOCUS; GENE MUTATION; GENE SEQUENCE; GENETIC MARKER; GENETIC SCREENING; GENOME ANALYSIS; HEARING IMPAIRMENT; HETEROZYGOSITY; HOMOZYGOSITY; HUMAN; JORDAN; MALE; MUTATIONAL ANALYSIS; PRIORITY JOURNAL; SCORING SYSTEM; SINGLE NUCLEOTIDE POLYMORPHISM;

CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 10; CONNEXINS; FAMILY; HAPLOTYPES; HEARING LOSS; HUMANS; INTRACELLULAR SIGNALING PEPTIDES AND PROTEINS; LINKAGE (GENETICS); LOD SCORE; MICROSATELLITE REPEATS; POLYMERASE CHAIN REACTION; POLYMORPHISM, SINGLE NUCLEOTIDE; POTASSIUM CHANNELS; SEQUENCE ANALYSIS, DNA;

EID: 57649185370     PISSN: 10184813     EISSN: 14765438     Source Type: Journal    
DOI: 10.1038/ejhg.2008.155     Document Type: Article

References (8)

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