一名患有纯合性变异型卟啉症的英国患者原卟啉原氧化酶缺乏R59W南非奠基者效应突变。 - Suppr | 超能文献

Lack of the R59W South African founder effect mutation in protoporphyrinogen oxidase in a British patient with homozygous variegate porphyria.

作者信息

McGrath J A, Hawk J L, Graham R M, Christiano A M

出版信息

Br J Dermatol. 1997 Feb;136(2):292. doi: 10.1111/j.1365-2133.1997.tb14923.x.

DOI:10.1111/j.1365-2133.1997.tb14923.x

Abstract

摘要

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