Mutations of the human P gene associated with Type II oculocutaneous albinism (OCA2). Mutations in brief no. 205. Online.

Human mutation

Volumn 12, Issue 6, 1998, Pages 434-

  Oetting, W S ^a   Gardner, J M ^a   Fryer, J P ^a   Ching, A ^a   Durham Pierre, D ^a   King, R A ^a   Brilliant, M H ^a  

^a UNIVERSITY OF MINNESOTA MEDICAL SCHOOL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CARRIER PROTEIN; MEMBRANE PROTEIN; OCA2 PROTEIN, HUMAN;

ARTICLE; GENETICS; HUMAN; MUTATION; OCULAR ALBINISM;

ALBINISM, OCULOCUTANEOUS; CARRIER PROTEINS; HUMANS; MEMBRANE PROTEINS; MEMBRANE TRANSPORT PROTEINS; MUTATION;

MLCS; MLOWN;

EID: 0005349251     PISSN: 10597794     EISSN: None     Source Type: Journal    
DOI: 10.1002/(sici)1098-1004(1998)12:6<434::aid-humu15>3.0.co;2-a     Document Type: Article

References (0)