The molecular basis of porphyria cutanea tarda in Chile: Identification and functional characterization of mutations in the uroporphyrinogen decarboxylase gene-Reference-Cited by-同舟云学术

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The molecular basis of porphyria cutanea tarda in Chile: Identification and functional characterization of mutations in the uroporphyrinogen decarboxylase gene

Published:2004-06 Issue:6 Volume:13 Page:372-379
ISSN:0906-6705
Container-title:Experimental Dermatology
language:en
Short-container-title:Exp Dermatol

Author:

Poblete-Gutierrez Pamela,Mendez Manuel,Wiederholt Tonio,Merk Hans F.,Fontanellas Antonio,Wolff Carlos,Frank Jorge

Publisher

Wiley

Subject

Dermatology,Molecular Biology,Biochemistry

Reference44 articles.

1. Familial and sporadic porphyria cutanea

2. Porphyria cutanea tarda

3. Genetics and pathogenesis of human uroporphyrinogen decarboxylase defects

Cited by 16 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Computational analysis of non-synonymous single nucleotide polymorphism in UROD gene linked with familial Porphyria Cutanea Tarda;Gene Reports;2021-12

2. Porphyria cutanea tarda: an intriguing genetic disease and marker;International Journal of Dermatology;2017-03-21

3. Porphyria cutanea tarda;Der Hautarzt;2016-01-07

4. Distribution and Quantitation of Skin Iron in Primary Haemochromatosis: Correlation with Total Body Iron Stores in Patients Undergoing Phlebotomy;Acta Dermato Venereologica;2014

5. Cutaneous porphyrias part I: epidemiology, pathogenesis, presentation, diagnosis, and histopathology;International Journal of Dermatology;2013-11-21

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