Mutation in and lack of expression of tyrosinase-related protein-1 (TRP- 1) in melanocytes from an individual with brown oculocutaneous albinism: A new subtype of albinism classified as 'OCA3'

American Journal of Human Genetics

Volumn 58, Issue 6, 1996, Pages 1145-1156

  Boissy, R E ^a   Zhao, H ^a   Oetting, W S ^a   Austin, L M ^a   Wildenberg, S C ^a   Boissy, Y L ^a   Zhao, Y ^a   Sturm, R A ^a   Hearing, V J ^a   King, R A ^a   Nordlund, J J ^a  

^a UNIVERSITY OF CINCINNATI COLLEGE OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENTARY DNA; GLYCINE CLEAVAGE SYSTEM; MELANIN; MONOPHENOL MONOOXYGENASE;

ARTICLE; CASE REPORT; CONTROLLED STUDY; DISEASE CLASSIFICATION; ENZYME ACTIVITY; GENE MAPPING; GENE MUTATION; HUMAN; HUMAN CELL; MALE; MELANOCYTE; MELANOGENESIS; NEGRO; NEWBORN; OCULOCUTANEOUS ALBINISM; PHENOTYPE; PRIORITY JOURNAL;

ALBINISM, OCULOCUTANEOUS; BASE SEQUENCE; CELLS, CULTURED; DIHYDROXYPHENYLALANINE; DISEASES IN TWINS; DNA PRIMERS; EXONS; FLUORESCENT ANTIBODY TECHNIQUE, INDIRECT; HOMOZYGOTE; HUMANS; MALE; MELANOCYTES; MEMBRANE GLYCOPROTEINS; MOLECULAR SEQUENCE DATA; MONOPHENOL MONOOXYGENASE; OXIDOREDUCTASES; POLYMERASE CHAIN REACTION; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; PROTEINS; SEQUENCE DELETION; SKIN; TWINS, DIZYGOTIC; TYROSINE 3-MONOOXYGENASE;

OXALIS TUBEROSA;

EID: 0029886028     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (0)