SLC40A1 and CP single nucleotide polymorphisms in porphyria cutanea tarda patients of mixed ancestry-Reference-Cited by-同舟云学术

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SLC40A1 and CP single nucleotide polymorphisms in porphyria cutanea tarda patients of mixed ancestry

Published:2018-05-17 Issue:5 Volume:82 Page:300-303
ISSN:0003-4800
Container-title:Annals of Human Genetics
language:en
Short-container-title:Annals of Human Genetics

Author:

Succi Isabella Brasil¹^ORCID,Pôrto Luís Cristóvão²,Silva Dayse³,Nascimento Adriana²,Neto Ronald Costa²,Fonseca João Carlos¹

Affiliation:

1. Dermatology Department Rio de Janeiro State University Rio de Janeiro Brazil

2. Histocompatibility and Criopreservation Laboratory Rio de Janeiro State University Rio de Janeiro Brazil

3. DNA Diagnostic Laboratory Rio de Janeiro State University Rio de Janeiro Brazil

Funder

Fundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro

Conselho Nacional de Desenvolvimento Científico e Tecnológico

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/ahg.12253

Reference15 articles.

1. The porphyrias: advances in diagnosis and treatment

2. Hemochromatosis genes and other factors contributing to the pathogenesis of porphyria cutanea tarda

3. Mutations in the hemochromatosis gene, porphyria cutanea tarda, and iron overload

4. Next-generation sequencing of hereditary hemochromatosis-related genes: Novel likely pathogenic variants found in the Portuguese population

5. The D519G Polymorphism of Glyceronephosphate O-Acyltransferase Is a Risk Factor for Familial Porphyria Cutanea Tarda

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