Evidence of a single origin for the most frequent mutation (R402W) causing glutaryl-CoA dehydrogenase deficiency: Identification of 3 novel polymorphisms and haplotype definition Communicated by: R.G.H. Cotton Online Citation: Human Mutation, Mutation in Brief #291 (1999) Online http://journals.wiley.com/1059-7794/pdf/mutation/291.pdf
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