P gene mutations associated with oculocutaneous albinism type II (OCA2).

Human mutation

Volumn 25, Issue 3, 2005, Pages 323-

  Oetting, William S ^a   Garrett, Sarah Savage ^a   Brott, Marcia ^a   King, Richard A ^a  

^a UNIVERSITY OF MINNESOTA MEDICAL SCHOOL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CARRIER PROTEIN; OCA2 PROTEIN, HUMAN;

AMINO ACID SUBSTITUTION; ARTICLE; ASIAN; CAUCASIAN; CLASSIFICATION; ETHNOLOGY; EUROPE; EXON; EYE COLOR; FEMALE; FRAMESHIFT MUTATION; GENE DELETION; GENETIC POLYMORPHISM; GENETICS; GENOTYPE; HAIR COLOR; HISPANIC; HUMAN; INFANT; JEW; MALE; MISSENSE MUTATION; NUCLEOTIDE SEQUENCE; OCULAR ALBINISM; PHILIPPINES; POINT MUTATION; PRESCHOOL CHILD; RNA SPLICING; STOP CODON;

ALBINISM, OCULOCUTANEOUS; AMINO ACID SUBSTITUTION; ASIAN CONTINENTAL ANCESTRY GROUP; CHILD, PRESCHOOL; CODON, NONSENSE; DNA MUTATIONAL ANALYSIS; EUROPE; EUROPEAN CONTINENTAL ANCESTRY GROUP; EXONS; EYE COLOR; FEMALE; FRAMESHIFT MUTATION; GENOTYPE; HAIR COLOR; HISPANIC AMERICANS; HUMANS; INFANT; JEWS; MALE; MEMBRANE TRANSPORT PROTEINS; MUTATION, MISSENSE; PHILIPPINES; POINT MUTATION; POLYMORPHISM, GENETIC; RNA SPLICE SITES; SEQUENCE DELETION;

EID: 29444456332     PISSN: None     EISSN: 10981004     Source Type: Journal    
DOI: 10.1002/humu.9318     Document Type: Article

References (0)