Genetic mapping of hph2, a mutation affecting amino acid transport in the mouse
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics
Link
http://link.springer.com/content/pdf/10.1007/s003359900366.pdf
Reference34 articles.
1. Arriza JL, Kavanaugh MP, Fairman, WA, Wu Y-N, Murdoch GH, North RA, Amara SG (1993) Cloning and expression of a human neutral amino acid transporter with structural similarity to the glutamate transporter gene family. J Biol Chem 268, 15329–15332
2. Barlow DP (1994) Imprinting: a gamete’s point of view. Trends Genet 10, 194–199
3. Baron DN, Dent CE, Harris H, Hart EW, Jepson JB (1956) Hereditary pellagra-like skin rash with temporary cerebellar ataxia, constant renal amino-aciduria, and other bizarre biochemical features. Lancet 2, 421–428
4. Calonge MJ, Gasparini P, Chillaron J, Gallucci M, Rousaud F, Zelante L, Testar X, Dallapiccola B, DiSilverio F, Barcelo P, Estivill X, Zorzano A, Nunes V, Palacin M (1994) Cystinuria caused by mutations in rBAT, a gene involved in the transport of cystine. Nature Genet 6, 420–425
5. Cattanach BM, Beechey CV (1985) Differential activity of maternally and paternally derived chromosome regions in mice. Nature 315, 496–498
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