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Evidence of a single origin for the most frequent mutation (R402W) causing glutaryl-CoA dehydrogenase deficiency: Identification of 3 novel polymorphisms and haplotype definition
Christiane Busquets, M. Josep Coll, Antonia RibesVolume:
15
Year:
2000
Language:
english
Pages:
1
DOI:
10.1002/(sici)1098-1004(200002)15:23.0.co;2-f
File:
PDF, 18 KB
english, 2000