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Year | Number of Results |
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2002 | 1 |
2019 | 1 |
2020 | 2 |
2024 | 0 |
PubMed (OMIM) for id: 171019
3 results
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ADAMTS19-associated heart valve defects: Novel genetic variants consolidating a recognizable cardiac phenotype.
Clin Genet. 2020 Jul;98(1):56-63. doi: 10.1111/cge.13760. Epub 2020 May 19.
Clin Genet. 2020.
PMID: 32323311
Loss of ADAMTS19 causes progressive non-syndromic heart valve disease.
Wünnemann F, Ta-Shma A, Preuss C, Leclerc S, van Vliet PP, Oneglia A, Thibeault M, Nordquist E, Lincoln J, Scharfenberg F, Becker-Pauly C, Hofmann P, Hoff K, Audain E, Kramer HH, Makalowski W, Nir A, Gerety SS, Hurles M, Comes J, Fournier A, Osinska H, Robins J, Pucéat M; MIBAVA Leducq Consortium principal investigators; Elpeleg O, Hitz MP, Andelfinger G.
Wünnemann F, et al.
Nat Genet. 2020 Jan;52(1):40-47. doi: 10.1038/s41588-019-0536-2. Epub 2019 Dec 16.
Nat Genet. 2020.
PMID: 31844321
Free PMC article.
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Cloning, expression analysis, and structural characterization of seven novel human ADAMTSs, a family of metalloproteinases with disintegrin and thrombospondin-1 domains.
Cal S, Obaya AJ, Llamazares M, Garabaya C, Quesada V, López-Otín C.
Cal S, et al.
Gene. 2002 Jan 23;283(1-2):49-62. doi: 10.1016/s0378-1119(01)00861-7.
Gene. 2002.
PMID: 11867212
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