Connexin mutations and hearing loss [7]

Nature

Volumn 391, Issue 6662, 1998, Pages 32-

  Scott, D A ^a   Kraft, M L ^a   Stone, E M ^a   Sheffield, V C ^a   Smith, R J H ^a  

^a UNIVERSITY OF IOWA HOSPITALS AND CLINICS   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

GAP JUNCTION PROTEIN;

AMINO ACID SEQUENCE; AUTOSOMAL RECESSIVE DISORDER; BASE PAIRING; CHROMOSOME 13Q; DNA SEQUENCE; GENE MUTATION; HEARING LOSS; KERATOSIS PALMOPLANTARIS; LETTER; PRIORITY JOURNAL; SEQUENCE ANALYSIS; SINGLE STRAND CONFORMATION POLYMORPHISM;

ADULT; AGED; AGED, 80 AND OVER; CHROMOSOMES, HUMAN, PAIR 21; CONNEXINS; DATA INTERPRETATION, STATISTICAL; DEAFNESS; DNA MUTATIONAL ANALYSIS; FEMALE; HUMANS; MALE; MIDDLE AGED; PEDIGREE; POINT MUTATION;

EID: 0031933645     PISSN: 00280836     EISSN: None     Source Type: Journal    
DOI: 10.1038/34079     Document Type: Letter

References (6)