Functional associations of genetic variants involved in the clinical manifestation of erythropoietic protoporphyria in the Argentinean population
出版年份 2012 全文链接
标题
Functional associations of genetic variants involved in the clinical manifestation of erythropoietic protoporphyria in the Argentinean population
作者
关键词
-
出版物
JOURNAL OF THE EUROPEAN ACADEMY OF DERMATOLOGY AND VENEREOLOGY
Volume 27, Issue 6, Pages 754-762
出版商
Wiley
发表日期
2012-05-16
DOI
10.1111/j.1468-3083.2012.04566.x
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- Molecular epidemiology of erythropoietic protoporphyria in the U.K.
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- A homoallelic FECH mutation in a patient with both erythropoietic protoporphyria and palmar keratoderma
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- A homozygous mutation in the ferrochelatase gene underlies erythropoietic protoporphyria associated with palmar keratoderma
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- Unknown
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- Seasonal Palmar Keratoderma in Erythropoietic Protoporphyria Indicates Autosomal Recessive Inheritance
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- A 10376 bp deletion of FECH gene responsible for erythropoietic protoporphyria
- (2007) Elena Di Pierro et al. BLOOD CELLS MOLECULES AND DISEASES
- Identification of a ferrochelatase mutation in a Chinese family with erythropoietic protoporphyria
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