MC1R mutations modify the classic phenotype of oculocutaneous albinism type 2 (OCA2)

American Journal of Human Genetics

Volumn 73, Issue 3, 2003, Pages 638-645

  King, Richard A ^a,b   Willaert, Rebecca K ^a   Schmidt, Ramona M ^a   Pietsch, Jacy ^b   Savage, Sarah ^b   Brott, Marcia J ^b   Fryer, James P ^b   Summers, C Gail ^a,b   Oetting, William S ^a,b  

^a UNIVERSITY OF MINNESOTA   (United States)

^b UNIVERSITY OF MINNESOTA MEDICAL SCHOOL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

MELANIN; MELANOCORTIN 1 RECEPTOR;

ADOLESCENT; ADULT; ARTICLE; CHILD; CLINICAL ARTICLE; CONTROLLED STUDY; DEVELOPMENTAL DISORDER; DISEASE ASSOCIATION; DNA MODIFICATION; EYE DEVELOPMENT; FEMALE; GENE IDENTIFICATION; GENE LOCUS; GENE MUTATION; HAIR COLOR; HUMAN; HYPOPIGMENTATION; MALE; MULTIGENE FAMILY; OCULOCUTANEOUS ALBINISM; OCULOCUTANEOUS ALBINISM TYPE 2; PHENOTYPE; PRIORITY JOURNAL; SEQUENCE ANALYSIS;

OXALIS TUBEROSA;

EID: 0041886412     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/377569     Document Type: Article

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