Wikidata

(Q73389192)

English

Evidence of a single origin for the most frequent mutation (R402W) causing glutaryl-CoA dehydrogenase deficiency: identification of 3 novel polymorphisms and haplotype definition

scientific article published on 01 February 2000

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title
Evidence of a single origin for the most frequent mutation (R402W) causing glutaryl-CoA dehydrogenase deficiency: identification of 3 novel polymorphisms and haplotype definition (English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10649503
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10649503%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019

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