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10.1016/j.ajhg.2014.10.018

http://scihub22266oqcxt.onion/10.1016/j.ajhg.2014.10.018
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suck abstract from ncbi


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pmid25434006      Am+J+Hum+Genet 2014 ; 95 (6): 736-43
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  • MFAP5 Loss-of-Function Mutations Underscore the Involvement of Matrix Alteration in the Pathogenesis of Familial Thoracic Aortic Aneurysms and Dissections #MMPMID25434006
  • Barbier M; Gross MS; Aubart M; Hanna N; Kessler K; Guo DC; Tosolini L; Ho-Tin-Noe B; Regalado E; Varret M; Abifadel M; Milleron O; Odent S; Dupuis-Girod S; Faivre L; Edouard T; Dulac Y; Busa T; Gouya L; Milewicz D; Jondeau G; Boileau C
  • Am J Hum Genet 2014[Dec]; 95 (6): 736-43 PMID25434006show ga
  • Thoracic aortic aneurysm and dissection (TAAD) is an autosomal-dominant disorder with major life-threatening complications. The disease displays great genetic heterogeneity with some forms allelic to Marfan and Loeys-Dietz syndrome, and an important number of cases still remain unexplained at the molecular level. Through whole-exome sequencing of affected members in a large TAAD-affected family, we identified the c.472C>T (p.Arg158?) nonsense mutation in MFAP5 encoding the extracellular matrix component MAGP-2. This protein interacts with elastin fibers and the microfibrillar network. Mutation screening of 403 additional probands identified an additional missense mutation of MFAP5 (c.62G>T [p.Trp21Leu]) segregating with the disease in a second family. Functional analyses performed on both affected individual?s cells and in vitro models showed that these two mutations caused pure or partial haploinsufficiency. Thus, alteration of MAGP-2, a component of microfibrils and elastic fibers, appears as an initiating mechanism of inherited TAAD.
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