The molecular basis of medium chain acyl-CoA dehydrogenase deficiency: survey and evolution of 985A----G transition, and identification of five rare types of mutation within the medium chain acyl-CoA dehydrogenase gene.

I. Yokota, P. M. Coates, D. E. Hale, P. Rinaldo, K. Tanaka

Research output: Contribution to journalArticle

7 Citations (Scopus)
Original languageEnglish (US)
Pages (from-to)425-440
Number of pages16
JournalProgress in Clinical and Biological Research
Volume375
StatePublished - 1992
Externally publishedYes

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Molecular Sequence Data
Skin Physiological Phenomena
Fatty Acid Desaturases
Acyl-CoA Dehydrogenase
Inborn Errors Metabolism
Homozygote
Guanine
Adenine
Ethnic Groups
Restriction Fragment Length Polymorphisms
Cultured Cells
Fibroblasts
Alleles
Polymerase Chain Reaction
Mutation
Genes
Medium chain acyl CoA dehydrogenase deficiency
Surveys and Questionnaires

ASJC Scopus subject areas

  • Medicine(all)

Cite this

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title = "The molecular basis of medium chain acyl-CoA dehydrogenase deficiency: survey and evolution of 985A----G transition, and identification of five rare types of mutation within the medium chain acyl-CoA dehydrogenase gene.",
author = "I. Yokota and Coates, {P. M.} and Hale, {D. E.} and P. Rinaldo and K. Tanaka",
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journal = "Progress in Clinical and Biological Research",
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AU - Coates, P. M.

AU - Hale, D. E.

AU - Rinaldo, P.

AU - Tanaka, K.

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