@article{ef9df99e5fd24039ac969ccd085da9e1,
title = "Mapping of the l-methylmalonyl-CoA mutase gene to mouse chromosome 17",
abstract = "In humans, methylmalonyl acidemia is caused by a deficiency of l-methylmalonyl-CoA mutase (MUT) controlled by a gene that has been mapped to chromosome 6. The mouse homolog of this gene has now been mapped to mouse chromosome 17. Recombinant inbred and congenic strains place the mouse Mut locus 1.06 cM distal to H-2, between Pgk-2 and Ce-2. The relative order of syntenic probes flanking H-2 on mouse chromosome 17 and HLA on human chromosome 6 is shown to be different.",
author = "Jadranka Serti{\'c} and Vladimir Vincek and Ledley, {Fred D.} and Felipe Figueroa and Jan Klein",
note = "Funding Information: We are grateful to Dr. L. Flaherty and Dr. H. C. Passmore for providing us with congenic and recombinant strains. We thank Ms. Margarethe Wiirstle and Mr. My Tran for devoted technical assistance, as well as Ms. Lynne Yakes for editorial help. This work was supported in part by Grant 1 ROl AI23667 from the National Institutes of Health, Bethesda, Maryland, and Grant 163258 from the Verband der Chemischen Industrie, Frankfurt, FRG.",
year = "1990",
month = mar,
doi = "10.1016/0888-7543(90)90487-F",
language = "English (US)",
volume = "6",
pages = "560--564",
journal = "Genomics",
issn = "0888-7543",
publisher = "Academic Press Inc.",
number = "3",
}