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Volumn 17, Issue 4, 2001, Pages 351-
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Identification of a novel COCH mutation, I109N, highlights the similar clinical features observed in DFNA9 families.
a
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Author keywords
[No Author keywords available]
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Indexed keywords
COCH PROTEIN, HUMAN;
COCH PROTEIN, MOUSE;
PROTEIN;
ADULT;
AMINO ACID SEQUENCE;
ANIMAL;
ARTICLE;
AUSTRALIA;
DIZZINESS;
DOMINANT GENE;
GENETIC SCREENING;
GENETICS;
HETEROZYGOTE;
HUMAN;
INTERNET;
MIDDLE AGED;
MISSENSE MUTATION;
MOLECULAR GENETICS;
NUCLEOTIDE SEQUENCE;
ONSET AGE;
PATHOPHYSIOLOGY;
PEDIGREE;
PERCEPTION DEAFNESS;
PHENOTYPE;
POINT MUTATION;
POLYMERASE CHAIN REACTION;
SEQUENCE ALIGNMENT;
ADULT;
AGE OF ONSET;
AMINO ACID SEQUENCE;
ANIMALS;
AUSTRALIA;
DIZZINESS;
DNA MUTATIONAL ANALYSIS;
GENES, DOMINANT;
GENETIC SCREENING;
HEARING LOSS, SENSORINEURAL;
HETEROZYGOTE;
HUMANS;
INTERNET;
MIDDLE AGED;
MOLECULAR SEQUENCE DATA;
MUTATION, MISSENSE;
PEDIGREE;
PHENOTYPE;
POINT MUTATION;
POLYMERASE CHAIN REACTION;
PROTEINS;
SEQUENCE ALIGNMENT;
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EID: 18044401372
PISSN: None
EISSN: 10981004
Source Type: Journal
DOI: 10.1002/humu.37 Document Type: Article |
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Times cited : (58)
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References (0)
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