日本人先天性第XIII因子Aサブユニット欠損症に認められた2つの点突然変異の検出  [in Japanese] Identification of Two Point Mutations in Japanese Patients with Congenital Coagulation Factor XIII A Subunit Deficiencies Novel Missense Mutation (Gly46lArg) and Nonsense Mutation (Arg66lStop)  [in Japanese]

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Author(s)

Journal

  • 日本血栓止血学会誌 = The Journal of Japanese Society on Thrombosis and Hemostasis

    日本血栓止血学会誌 = The Journal of Japanese Society on Thrombosis and Hemostasis 9(2), 110-119, 1998-04-01

References:  24

Cited by:  1

Codes

  • NII Article ID (NAID)
    10008632362
  • NII NACSIS-CAT ID (NCID)
    AN10353762
  • Text Lang
    JPN
  • Article Type
    Journal Article
  • ISSN
    09157441
  • Data Source
    CJP  CJPref 
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