Missense mutation in keratin 17 cause either pachyonychia congenita type 2 or a phenotype resembling steatocystoma multiplex

• SMITH FJD

収録刊行物

• J Invest Dermatol

  J Invest Dermatol 108 220-223, 1997

詳細情報

• CRID: 1573387450854928512
• NII論文ID: 30014534595
• NII書誌ID: AA00700733
• DOI: 10.1111/1523-1747.ep12335315
• データソース種別:
  • CiNii Articles