@article{e90106b58f1549af93897dad947bd3b7,
title = "A polymorphic synonymous mutation in human ornithine-δ-aminotransferase (N378N)",
author = "Martin, {Laura S.} and Mitchell, {Grant A.} and Jacques Michaud and Brody, {Lawrence C.} and David Valle",
note = "Funding Information: Acknowledgements: This work was supported in part by a grant from the National Institutes of Health (EY02948) (DV) and a grant from the Steder Research Fund for Women Physicians (LM). GM was supported by the Fonds de la Recherche en Sante du Quebec and the Medical Research Council of Canada. LB and DV are supported by the Howard Hughes Medical Institute. Funding Information: Not Polymorphic For. Not applicable. Chromosomal Localization: Not applicable. Mendelian Inheritance: Strictly maternal inheritance in a pedigree of 30 individuals. Probe Availability: Not applicable. Other Comments: Not applicable. Acknowledgements: This work was supported by a grant of the Diabetes Fonds Nederland. References: l)Holt,I.J. et al. (1988) Hum. Genet. 79, 53-57. 2)Anderson,S. et al. (1981) Nature 290, 457-465.",
year = "1991",
month = apr,
day = "25",
doi = "10.1093/nar/19.8.1962",
language = "English (US)",
volume = "19",
pages = "1962",
journal = "Nucleic Acids Research",
issn = "1362-4962",
publisher = "Oxford University Press",
number = "8",
}