Literature DB >> 7545057

Integrin beta 4 mutations associated with junctional epidermolysis bullosa with pyloric atresia.

F Vidal1, D Aberdam, C Miquel, A M Christiano, L Pulkkinen, J Uitto, J P Ortonne, G Meneguzzi.   

Abstract

Pyloric atresia associated with junctional epidermolysis bullosa (PA-JEB), is a rare inherited disorder characterized by pyloric stenosis and blistering of the skin as primary manifestations. We demonstrate that in one PA-JEB patient the disease resulted from two distinct mutations in the beta 4 integrin gene alleles. The paternal mutation consists of a one base pair deletion causing a shift in the open reading frame, and a downstream premature termination codon. The maternal mutation occurs in a donor splice site, and results in in-frame exon skipping involving the cytoplasmic domain of the polypeptide. Our results implicate mutations in the beta 4 integrin gene in some forms of PA-JEB.

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Year:  1995        PMID: 7545057     DOI: 10.1038/ng0695-229

Source DB:  PubMed          Journal:  Nat Genet        ISSN: 1061-4036            Impact factor:   38.330


  69 in total

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6.  First successful preimplantation genetic diagnosis of epidermolysis bullosa with pyloric atresia: case study of a novel c.4505-4508insACTC mutation.

Authors:  Ayvaz Ozge; Hatırnaz Safak; Hatırnaz Ebru; Unsal Evrim; Sinanoglu Ekin Bilge; Ozer Leyla; Kadı Ali Kemal; Baltacı Volkan
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Review 7.  Stomach development, stem cells and disease.

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Authors:  Michael E Werner; Feng Chen; Jose V Moyano; Fruma Yehiely; Jonathan C R Jones; Vincent L Cryns
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9.  Mutations in capillary morphogenesis gene-2 result in the allelic disorders juvenile hyaline fibromatosis and infantile systemic hyalinosis.

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10.  Specificity of binding of the plectin actin-binding domain to beta4 integrin.

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Journal:  Mol Biol Cell       Date:  2003-07-11       Impact factor: 4.138

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