[Updated on Apr. 18] Integration of CiNii Articles into CiNii Research

Two point mutations within the coproporphyrinogen oxidase gene in a child with symptomatic hereditary coproporphyria.

Bibliographic Information

Title
Two point mutations within the coproporphyrinogen oxidase gene in a child with symptomatic hereditary coproporphyria.
Author
Niizuma T, Terada K, Nakajima M, Daimon Y, Inoue M, Ogita S, Kataoka N

Journal

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Details

  • CRID
    1010282257431029896
  • Article Type
    journal article
  • Data Source
    • KAKEN

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