APC mutation associated with late onset of familial adenomatous polyposis.

Abstract : Familial adenomatous polyposis is an autosomal dominantly inherited disorder. Mutation studies in the corresponding gene (APC) may provide information for predictive tests for persons at risk in affected families. We report here a new mutation in exon 6 (codon 233) of the APC gene and clinical data in a large family with late onset of the disease in most affected persons. Images
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https://hal.univ-antilles.fr/hal-01700358
Contributor : Juliette Smith-Ravin <>
Submitted on : Sunday, February 4, 2018 - 4:41:08 AM
Last modification on : Wednesday, September 5, 2018 - 12:32:03 AM

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  • HAL Id : hal-01700358, version 1
  • PUBMEDCENTRAL : PMC1016666

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Juliette Smith-Ravin, R Smith-Ravin, K. Pack, S Hodgson, S Tay, et al.. APC mutation associated with late onset of familial adenomatous polyposis.. Journal of Medical Genetics, BMJ Publishing Group, 1970, 31 (11). ⟨hal-01700358⟩

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