A mutation causing Alport syndrome with tardive hearing loss is common in the western United States

American Journal of Human Genetics

Volumn 58, Issue 6, 1996, Pages 1157-1165

  Barker, D F ^a   Pruchno, C J ^a   Jiang, X ^a   Atkin, C L ^a   Stone, E M ^a   Denison, J C ^a   Fain, P R ^a   Gregory, M C ^a  

^a University of Utah Research Park   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENTARY DNA;

ADULT; ALPORT SYNDROME; ARTICLE; CHROMOSOME XQ; CLINICAL ARTICLE; CLINICAL FEATURE; CONTROLLED STUDY; FAMILY STUDY; FEMALE; GENE MUTATION; GENETIC LINKAGE; GEOGRAPHIC DISTRIBUTION; GLOMERULONEPHRITIS; HEARING LOSS; HUMAN; HUMAN CELL; MALE; ONSET AGE; PRIORITY JOURNAL; UNITED STATES; X CHROMOSOME INACTIVATION;

ADOLESCENT; ADULT; AGE FACTORS; AGED; BASE SEQUENCE; CHILD; COLLAGEN; DNA PRIMERS; FEMALE; HEARING LOSS; HETEROZYGOTE DETECTION; HUMANS; INCIDENCE; IOWA; KIDNEY FAILURE, CHRONIC; LINKAGE (GENETICS); MALE; MIDDLE AGED; MOLECULAR SEQUENCE DATA; NEPHRITIS, HEREDITARY; PEDIGREE; POINT MUTATION; RNA; SKIN; UNITED STATES; UTAH;

EID: 0029943825     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (0)