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Cardiac conduction defects associate with mutations in SCN5A.
Schott JJ, Alshinawi C, Kyndt F, Probst V, Hoorntje TM, Hulsbeek M, Wilde AA, Escande D, Mannens MM, Le Marec H. Schott JJ, et al. Among authors: mannens mm. Nat Genet. 1999 Sep;23(1):20-1. doi: 10.1038/12618. Nat Genet. 1999. PMID: 10471492 No abstract available.
KVLQT1, the rhythm of imprinting.
Mannens M, Wilde A. Mannens M, et al. Nat Genet. 1997 Feb;15(2):113-5. doi: 10.1038/ng0297-113. Nat Genet. 1997. PMID: 9020829 No abstract available.
A dominant negative isoform of the long QT syndrome 1 gene product.
Demolombe S, Baró I, Péréon Y, Bliek J, Mohammad-Panah R, Pollard H, Morid S, Mannens M, Wilde A, Barhanin J, Charpentier F, Escande D. Demolombe S, et al. J Biol Chem. 1998 Mar 20;273(12):6837-43. doi: 10.1074/jbc.273.12.6837. J Biol Chem. 1998. PMID: 9506986 Free article.
[Iatrogenic collapse; can this be prevented?].
Wilde AA, Mannens MM. Wilde AA, et al. Among authors: mannens mm. Ned Tijdschr Geneeskd. 1997 Apr 19;141(16):796-7. Ned Tijdschr Geneeskd. 1997. PMID: 9213809 Dutch. No abstract available.
A single Na(+) channel mutation causing both long-QT and Brugada syndromes.
Bezzina C, Veldkamp MW, van Den Berg MP, Postma AV, Rook MB, Viersma JW, van Langen IM, Tan-Sindhunata G, Bink-Boelkens MT, van Der Hout AH, Mannens MM, Wilde AA. Bezzina C, et al. Among authors: mannens mm. Circ Res. 1999 Dec 3-17;85(12):1206-13. doi: 10.1161/01.res.85.12.1206. Circ Res. 1999. PMID: 10590249
Mutations in ZBTB20 cause Primrose syndrome.
Cordeddu V, Redeker B, Stellacci E, Jongejan A, Fragale A, Bradley TE, Anselmi M, Ciolfi A, Cecchetti S, Muto V, Bernardini L, Azage M, Carvalho DR, Espay AJ, Male A, Molin AM, Posmyk R, Battisti C, Casertano A, Melis D, van Kampen A, Baas F, Mannens MM, Bocchinfuso G, Stella L, Tartaglia M, Hennekam RC. Cordeddu V, et al. Among authors: mannens mm. Nat Genet. 2014 Aug;46(8):815-7. doi: 10.1038/ng.3035. Epub 2014 Jul 13. Nat Genet. 2014. PMID: 25017102
192 results