A new locus for nonsyndromic deafness DFNB49 maps to chromosome 5q12.3-q14.1

Human Genetics

Volumn 116, Issue 1-2, 2005, Pages 17-22

  Ramzan, Khushnooda ^a   Shaikh, Rehan S ^a   Ahmad, Jamil ^a   Khan, Shaheen N ^a   Riazuddin, Saima ^a,b   Ahmed, Zubair M ^b   Friedman, Thomas B ^b   Wilcox, Edward R ^b   Riazuddin, Sheikh ^b  

^a UNIVERSITY OF THE PUNJAB   (Pakistan)

^b NATIONAL INSTITUTES OF HEALTH   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

GENOMIC DNA; OCCLUDIN; RNA POLYMERASE II; TRANSCRIPTION FACTOR; ZINC TRANSPORTER;

ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CHROMOSOME 5Q; CHROMOSOME BAND; CHROMOSOME MAP; CHROMOSOME MARKER; CHROMOSOME MUTATION; CHROMOSOME SEGREGATION; CONGENITAL DEAFNESS; CONTROLLED STUDY; DNA DETERMINATION; DNA FLANKING REGION; EXON; FAMILY STUDY; GENE LOCUS; GENETIC CODE; GENETIC HETEROGENEITY; GENETIC LINKAGE; GENETIC RECOMBINATION; HAPLOTYPE; HETEROZYGOTE; HUMAN; PAKISTAN; PRIORITY JOURNAL; SEQUENCE ANALYSIS;

AUDIOMETRY; CHROMOSOME MAPPING; CONSANGUINITY; DEAFNESS; FEMALE; GENES, RECESSIVE; GENETIC MARKERS; HUMANS; MALE; PEDIGREE;

EID: 11244305469     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00439-004-1205-8     Document Type: Article

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