A molecular defect in human protoporphyria.

Brenner, D A; Didier, J M; Frasier, F; Christensen, S R; Evans, G A; Dailey, H A

Brenner, D A; Didier, J M; Frasier, F; Christensen, S R; Evans, G A; Dailey, H A.

Affiliation

Brenner DA; Department of Medicine, UCSD, La Jolla 92093-0623.

Am J Hum Genet ; 50(6): 1203-10, 1992 Jun.

Article in En | MEDLINE | ID: mdl-1376018

Subject(s)

Chromosomes, Human, Pair 18; Ferrochelatase/genetics; Mutation; Porphyrias/genetics; Amino Acid Sequence; Base Sequence; Blotting, Northern; Cell Line; Chromosome Banding; Chromosome Mapping; DNA/genetics; Ferrochelatase/metabolism; Humans; Hybrid Cells/physiology; Molecular Sequence Data; Oligodeoxyribonucleotides; Polymerase Chain Reaction/methods; Protoporphyrins/metabolism; RNA/genetics; RNA/isolation & purification

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Porphyrias / Chromosomes, Human, Pair 18 / Ferrochelatase / Mutation Limits: Humans Language: En Journal: Am J Hum Genet Year: 1992 Document type: Article Country of publication: United States

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