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Article

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

Mammalian genome : official journal of the International Mammalian Genome Society - 1 Feb 1997

Symula D J, Shedlovsky A, Dove W F

Abstract excerpt

We describe the genetic mapping of hyperphenylal-aninemia 2 (hph2), a recessive mutation in the mouse that causes deficient amino acid transport similar to Hartnup disorder, a human genetic amino acid transport disorder. The hph2 locus was mapped in three separate crosses to identify candidate genes for hph2 and a region of homology in the human genome where we propose the Hartnup Disorder gene might lie. The...

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PMID: 9060407
DOI: 10.1007/s003359900366

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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