About: Is hepatoerythropoietic porphyria a homozygous form of porphyria cutanea tarda? Inheritance of uroporphyrinogen decarboxylase deficiency in a Spanish family

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About: Is hepatoerythropoietic porphyria a homozygous form of porphyria cutanea tarda? Inheritance of uroporphyrinogen decarboxylase deficiency in a Spanish family Goto Sponge NotDistinct Permalink

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scientific article published on 01 May 1984

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в травні 1984 (uk) article scientifique publié en 1984 (fr) artículu científicu espublizáu en mayu de 1984 (ast) im Mai 1984 veröffentlichter wissenschaftlicher Artikel (de) scientific article published on 01 May 1984 (en)
publication date	wds:Q71348234-F2D8E5F3-B0AD-4B62-A1DB-2206738F4B88
publication date	1984-05-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q71348234-E958DCD2-10B2-46F2-9DF4-A7A4CACDFBD8
language of work or name	English
author name string	wds:Q71348234-6AD41C9F-E35B-47B1-9D02-5DFC022E3E3F wds:Q71348234-6D9BE199-8308-4D25-BC82-AF062A0D8FAA wds:Q71348234-6EF10FEA-B99E-4367-A9D4-823349CF39AD wds:Q71348234-C8E0B66A-A0E7-4D9A-9F56-2060F5F4C230 wds:Q71348234-F3A4250B-27C7-4C66-966C-36DF4DEC84A2 wds:Q71348234-F6B0412E-2FB1-4BB7-AA9F-C7ED44D11E11
author name string	G H Elder S Chinarro R E de Salamanca G Jaqueti M L Villaseca P Lazaro
rdfs:label	Is hepatoerythropoietic porphyria a homozygous form of porphyria cutanea tarda? Inheritance of uroporphyrinogen decarboxylase deficiency in a Spanish family (en) Is hepatoerythropoietic porphyria a homozygous form of porphyria cutanea tarda? Inheritance of uroporphyrinogen decarboxylase deficiency in a Spanish family (nl)
skos:prefLabel	Is hepatoerythropoietic porphyria a homozygous form of porphyria cutanea tarda? Inheritance of uroporphyrinogen decarboxylase deficiency in a Spanish family (en) Is hepatoerythropoietic porphyria a homozygous form of porphyria cutanea tarda? Inheritance of uroporphyrinogen decarboxylase deficiency in a Spanish family (nl)
name	Is hepatoerythropoietic porphyria a homozygous form of porphyria cutanea tarda? Inheritance of uroporphyrinogen decarboxylase deficiency in a Spanish family (en) Is hepatoerythropoietic porphyria a homozygous form of porphyria cutanea tarda? Inheritance of uroporphyrinogen decarboxylase deficiency in a Spanish family (nl)
title	wds:Q71348234-C94B79A6-4427-4AA8-A46E-B5CB36F9A1DB
title	Is hepatoerythropoietic porphyria a homozygous form of porphyria cutanea tarda? Inheritance of uroporphyrinogen decarboxylase deficiency in a Spanish family (en)
page(s)	wds:Q71348234-FBCC9ADE-C921-4F63-BE39-E0D16E1A0548
page(s)	613-617
instance of	wds:Q71348234-F7D842BD-9472-4E79-B1FA-10A6C3C9310D
instance of	scholarly article
main subject	wds:Q71348234-C242FDF0-F97B-420D-91ED-B866DE08F151 wds:Q71348234-C8DDC402-8975-4D6E-A3F8-EC0B4B22ADAC
main subject	hepatoerythropoietic porphyria homozygosity
PubMed ID	wds:Q71348234-0FA36C41-20F8-4B85-A313-15946B8814F0
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/6722030
PubMed ID	6722030
published in	wds:Q71348234-E5F8838B-79B0-4787-A646-08A690FFE4C3
published in	British Journal of Dermatology
issue	wds:Q71348234-99E3D2FE-589A-4D7A-A506-F32A20B6AC05
volume	wds:Q71348234-E9B7EE9A-3F17-4EE3-A28A-10F19B61430F
issue	5
volume	110
DOI	wds:Q71348234-8CFD43BB-0BC3-4464-AB54-273B85BAD080
DOI	http://dx.doi.org/10.1111/J.1365-2133.1984.TB04687.X
DOI	10.1111/J.1365-2133.1984.TB04687.X
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q71348234
is cites work of	Characterization of a new mutation (R292G) and a deletion at the human uroporphyrinogen decarboxylase locus in two patients with hepatoerythropoietic porphyria Immunochemical study of uroporphyrinogen decarboxylase in a patient with mild hepatoerythropoietic porphyria Mouse uroporphyrinogen decarboxylase: cDNA cloning, expression, and mapping Porphyria Diagnostics-Part 1: A Brief Overview of the Porphyrias Hepatoerythropoietic porphyria misdiagnosed as child abuse: cutaneous, arthritic, and hematologic manifestations in siblings with a novel UROD mutation Hepatoerythropoietic porphyria precipitated by viral hepatitis Molecular analysis of uroporphyrinogen decarboxylase deficiency in a family with two cases of hepatoerythropoietic porphyria Prevalence of the 281 (Gly----Glu) mutation in hepatoerythropoietic porphyria and porphyria cutanea tarda
is cites work of	wds:Q28118865-BF35EE91-36CB-4817-A290-824C2430ED8F wds:Q28590365-EED31111-5242-44D7-84F3-96A3BB17B43F wds:Q34974542-B34C5821-3E0F-441E-9F83-022BA3916413 wds:Q34377682-AB3211CC-5583-4813-A685-52A3B779E1E7 wds:Q36267789-FCB7336B-486C-4989-97D3-171BADC9B80E wds:Q69912015-0E0523C4-9D03-477B-9078-21A944588DAC wds:Q34572781-B0FC35B4-36C7-4D85-A01C-B647C223109B wds:Q34520576-56509E71-925F-4597-85E3-4CB88E727CE0

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