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Familial Porphyria Cutanea Tarda: Hybridization Analysis of the Uroporphyrinogen Decarboxylase Locus
Familial porphyria cutanea tarda (PCT) results from a deficiency of uroporphyrinogen decarboxylase (URO-D) activity. Hybridization analysis of genomic DNA from unrelated normal individuals and PCT pedigree members failed to detect any major deletions, rearrangements or restriction fragment length po...
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Published in: | Human heredity 1988, Vol.38 (5), p.283-286 |
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container_end_page | 286 |
container_issue | 5 |
container_start_page | 283 |
container_title | Human heredity |
container_volume | 38 |
creator | Hansen, Joanna L. O'Connell, Peter Romana, Marc Romeo, Paul-Henri Kushner, James P. |
description | Familial porphyria cutanea tarda (PCT) results from a deficiency of uroporphyrinogen decarboxylase (URO-D) activity. Hybridization analysis of genomic DNA from unrelated normal individuals and PCT pedigree members failed to detect any major deletions, rearrangements or restriction fragment length polymorphisms at the URO-D locus. |
doi_str_mv | 10.1159/000153800 |
format | article |
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Hybridization analysis of genomic DNA from unrelated normal individuals and PCT pedigree members failed to detect any major deletions, rearrangements or restriction fragment length polymorphisms at the URO-D locus.</description><identifier>ISSN: 0001-5652</identifier><identifier>EISSN: 1423-0062</identifier><identifier>DOI: 10.1159/000153800</identifier><identifier>PMID: 2906904</identifier><identifier>CODEN: HUHEAS</identifier><language>eng</language><publisher>Basel, Switzerland: S. Karger</publisher><subject>Base Sequence ; Biological and medical sciences ; Carboxy-Lyases - genetics ; DNA ; Humans ; Medical sciences ; Metabolic diseases ; Nucleic Acid Hybridization ; Original Paper ; Original Papers ; Other metabolic disorders ; Pigments (porphyrias, hyperbilirubinemias...) ; Polymorphism, Restriction Fragment Length ; Porphyrias - genetics ; Restriction Mapping ; Skin Diseases - genetics ; Uroporphyrinogen Decarboxylase - blood ; Uroporphyrinogen Decarboxylase - genetics</subject><ispartof>Human heredity, 1988, Vol.38 (5), p.283-286</ispartof><rights>1988 S. 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Hybridization analysis of genomic DNA from unrelated normal individuals and PCT pedigree members failed to detect any major deletions, rearrangements or restriction fragment length polymorphisms at the URO-D locus.</description><subject>Base Sequence</subject><subject>Biological and medical sciences</subject><subject>Carboxy-Lyases - genetics</subject><subject>DNA</subject><subject>Humans</subject><subject>Medical sciences</subject><subject>Metabolic diseases</subject><subject>Nucleic Acid Hybridization</subject><subject>Original Paper</subject><subject>Original Papers</subject><subject>Other metabolic disorders</subject><subject>Pigments (porphyrias, hyperbilirubinemias...)</subject><subject>Polymorphism, Restriction Fragment Length</subject><subject>Porphyrias - genetics</subject><subject>Restriction Mapping</subject><subject>Skin Diseases - genetics</subject><subject>Uroporphyrinogen Decarboxylase - blood</subject><subject>Uroporphyrinogen Decarboxylase - genetics</subject><issn>0001-5652</issn><issn>1423-0062</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1988</creationdate><recordtype>article</recordtype><recordid>eNptkM9LwzAcxYMoOqcH7woBUfBQTdKmab3J_DFhoAc9l2_TZMvsmpq0YP3r7ViZIJ5C8j7f9817CJ1Qck0pT28IIZSHCSE7aEQjFgaExGwXjdbvAY85O0CH3i_7a0JEuI_2WUrilEQjVDzCypQGSvxqXb3onAE8aRuoFOA3cAXc4mmXO1OYb2iMrfBdBWXnjcdW42ah8Luz9TBZ2bmq8L2S4HL71ZXgFZ5Z2fojtKeh9Op4OMfo_fHhbTINZi9Pz5O7WSDDiDaBpikHTqQSmnOZM8YUi8IopjmXIIAXiSQaQOkCIhWSWCeQpn3SOM9FoqkOx-hy41s7-9kq32Qr46Uqyz6ObX0mEkGjfqIHrzagdNZ7p3RWO7MC12WUZOtGs22jPXs2mLb5ShVbcqiw1y8GHbyEUjuopPG_hikTnDLRc-cb7gPcXLktMJ0-bDZldbGOcPov9fczS9_YXzXilDBGRfgDAp2dDw</recordid><startdate>1988</startdate><enddate>1988</enddate><creator>Hansen, Joanna L.</creator><creator>O'Connell, Peter</creator><creator>Romana, Marc</creator><creator>Romeo, Paul-Henri</creator><creator>Kushner, James P.</creator><general>S. 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Hybridization analysis of genomic DNA from unrelated normal individuals and PCT pedigree members failed to detect any major deletions, rearrangements or restriction fragment length polymorphisms at the URO-D locus.</abstract><cop>Basel, Switzerland</cop><pub>S. Karger</pub><pmid>2906904</pmid><doi>10.1159/000153800</doi><tpages>4</tpages></addata></record> |
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ispartof | Human heredity, 1988, Vol.38 (5), p.283-286 |
issn | 0001-5652 1423-0062 |
language | eng |
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source | JSTOR Archival Journals and Primary Sources Collection |
subjects | Base Sequence Biological and medical sciences Carboxy-Lyases - genetics DNA Humans Medical sciences Metabolic diseases Nucleic Acid Hybridization Original Paper Original Papers Other metabolic disorders Pigments (porphyrias, hyperbilirubinemias...) Polymorphism, Restriction Fragment Length Porphyrias - genetics Restriction Mapping Skin Diseases - genetics Uroporphyrinogen Decarboxylase - blood Uroporphyrinogen Decarboxylase - genetics |
title | Familial Porphyria Cutanea Tarda: Hybridization Analysis of the Uroporphyrinogen Decarboxylase Locus |
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