Novel autosomal recessive nonsyndromic hearing impairment locus DFNB90 maps to 7p22.1-p15.3

Human Heredity

Volumn 71, Issue 2, 2011, Pages 106-112

  Ali, Ghazanfar ^a   Lee, Kwanghyuk ^b   Andrade, Paula B ^b   Basit, Sulman ^a   Santos Cortez, Regie Lyn P ^b   Chen, Leon ^b   Jelani, Musharraf ^a   Ansar, Muhammad ^a   Ahmad, Wasim ^a   Leal, Suzanne M ^b  

^a QUAID I AZAM UNIVERSITY   (Pakistan)

^b BAYLOR COLLEGE OF MEDICINE   (United States)

Author keywords

7p22.1 p15.3; Autosomal recessive; DFNA5; DFNB44; DFNB90; Nonsyndromic hearing impairment

Indexed keywords

BETA ACTIN; NUCLEIC ACID BINDING PROTEIN; ONCOMODULIN; RAC1 PROTEIN; REPLICATION PROTEIN A3; UNCLASSIFIED DRUG;

ARTICLE; AUTOSOMAL RECESSIVE DISORDER; AUTOSOMAL RECESSIVE NONSYNDROMIC HEARING IMPAIRMENT; CHROMOSOME 7; CHROMOSOME MAP; GENE LOCUS; GENE MAPPING; GENE SEQUENCE; GENETIC VARIABILITY; HEARING IMPAIRMENT; HOMOZYGOSITY; HUMAN; SINGLE NUCLEOTIDE POLYMORPHISM;

ACTINS; CALCIUM-BINDING PROTEINS; CELL CYCLE PROTEINS; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 7; CONSANGUINITY; DNA-BINDING PROTEINS; FEMALE; GENES, RECESSIVE; GENETIC LOCI; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; GLYCOPROTEINS; HAPLOTYPES; HEARING LOSS; HUMANS; MALE; NEUROPEPTIDES; PEDIGREE; POLYMORPHISM, SINGLE NUCLEOTIDE; PROMOTER REGIONS, GENETIC; RAC1 GTP-BINDING PROTEIN; RIBOSE-PHOSPHATE PYROPHOSPHOKINASE; SEQUENCE ANALYSIS, DNA; TRANSCRIPTION FACTORS;

EID: 79960129427     PISSN: 00015652     EISSN: 14230062     Source Type: Journal    
DOI: 10.1159/000320154     Document Type: Article

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