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迟发性皮肤卟啉病1例 被引量:2

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出处 《皮肤病与性病》 2008年第3期54-55,共2页 Dermatology and Venereology
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  • 1JamesWD,BergerTG,ElstonDM.安德鲁斯临床皮肤病学[M].10版.北京:科学出版社,2008:547-551.
  • 2杨国亮.皮肤病学[M].上海:上海科学技术文献出版社,2005.775.
  • 3Aarsand Aasne K,Boman Helge,Sandberg Sverre.Familial and sporadic porphyria cutanea tarda: characterization and diagnostic strategies. Clinical Chemistry . 2009
  • 4Phillips J D,Parker T L,Schubert H L,Whitby F G,Hill C P,Kushner J P.Functional consequences of naturally occurring mutations in human uroporphyrinogen decarboxylase. Blood . 2001
  • 5Helen Thadani,Allan Deacon,Timothy Pete.Regular review: Diagnosis and management of porphyria. British Medical Journal . 2000
  • 6Andrew G. Smith,George H. Elder.Complex Gene?Chemical Interactions: Hepatic Uroporphyria As a Paradigm. Chemical Research in Toxicology . 2010
  • 7M.D.Cappellini,F.Martinez di Montemuros,D.Tavazzi,S.Fargion,A.Pizzuti,A.Comino,T.Cainelli,G.Fiorelli.??Seven novel point mutations in the uroporphyrinogen decarboxylase (UROD) gene in patients with familial porphyria cutanea tarda (f‐PCT)(J)Hum. Mutat. . 2001 (4)
  • 8McManus J F,Begley C G,Sassa S,Ratnaike S.Five new mutations in the uroporphyrinogen decarboxylase gene identified in families with cutaneous porphyria. Blood . 1996
  • 9M.Méndez,P.Poblete‐Gutiérrez,M.García‐Bravo,T.Wiederholt,M.J.Morán‐Jiménez,H.F.Merk,M.C.Garrido‐Astray,J.Frank,A.Fontanellas,R.Enríquez de Salamanca.??Molecular heterogeneity of familial porphyria cutanea tarda in Spain: characterization of 10 novel mutations in the UROD gene(J)British Journal of Dermatology . 2007 (3)

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