C1 Inhibitor Gene Sequence Facilitates Frameshift Mutations

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C1 inhibitor gene sequence facilitates frameshift mutations.

Mutations disrupting the function or production of C1 inhibitor cause the disease hereditary angioneurotic edema. Patient mutations identified an imperfect inverted repeat sequence that was postulated to play a mechanistic role in the mutations. To test this hypothesis, the inverted repeat was cloned into the chloramphenicol acetyltransferase gene in pBR325 and its mutation rate was studied in ...

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CpG mutations in the reactive site of human C1 inhibitor.

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A cluster of mutations within a short triplet repeat in the C1 inhibitor gene.

Mutations in the C1 inhibitor gene that result in low functional levels of C1 inhibitor protein cause hereditary angioneurotic edema. This disease is characterized by episodic edema leading to considerable morbidity and death. Among 60 unreported kindred with the disease, four patients were discovered to have mutations clustered within a 12-bp segment of exon 5 from nucleotide 8449 to nucleotid...

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Expression of platelet C1 inhibitor.

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ژورنال

عنوان ژورنال: Molecular Medicine

سال: 1998

ISSN: 1076-1551,1528-3658

DOI: 10.1007/bf03401772