Genetic mapping of hph2, a mutation affecting amino acid transport in the mouse

Mammalian Genome

Volumn 8, Issue 2, 1997, Pages 98-101

  Symula, D J ^a,b   Shedlovsky, A ^a   Dove, W F ^b  

^a UNIVERSITY OF WISCONSIN MADISON   (United States)

^b UNIVERSITY OF WISCONSIN MADISON   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

PHENYLALANINE;

ANIMAL; ARTICLE; C57BL MOUSE; CHROMOSOME MAP; CROSS BREEDING; DISEASE MODEL; GENETICS; HARTNUP DISEASE; HUMAN; METABOLISM; MOUSE; MUTATION; TRANSPORT AT THE CELLULAR LEVEL;

ANIMALS; BIOLOGICAL TRANSPORT; CHROMOSOME MAPPING; CROSSES, GENETIC; DISEASE MODELS, ANIMAL; HARTNUP DISEASE; HUMANS; MICE; MICE, INBRED C57BL; MUTATION; PHENYLALANINE;

ANIMALIA; RODENTIA;

EID: 0031063191     PISSN: 09388990     EISSN: None     Source Type: Journal    
DOI: 10.1007/s003359900366     Document Type: Article

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