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CpG Methylation, a Parent-of-Origin Effect for Maternal-Biased Transmission of Congenital Myotonic Dystrophy.
Barbé L, Lanni S, López-Castel A, Franck S, Spits C, Keymolen K, Seneca S, Tomé S, Miron I, Letourneau J, Liang M, Choufani S, Weksberg R, Wilson MD, Sedlacek Z, Gagnon C, Musova Z, Chitayat D, Shannon P, Mathieu J, Sermon K, Pearson CE. Barbé L, et al. Among authors: musova z. Am J Hum Genet. 2017 Mar 2;100(3):488-505. doi: 10.1016/j.ajhg.2017.01.033. Am J Hum Genet. 2017. PMID: 28257691 Free PMC article.
[Genetic study of 20 patients with autism disorders].
Havlovicová M, Propper L, Novotná D, Musová Z, Hrdlicka M, Sedlácek Z. Havlovicová M, et al. Among authors: musova z. Cas Lek Cesk. 2002 Jun 21;141(12):381-7. Cas Lek Cesk. 2002. PMID: 12238024 Czech.
Myotonic dystrophy type 2 and multiple sclerosis: case report.
Ehler E, Novotná A, Mareš M, Mušová Z, Mrklovský M. Ehler E, et al. Among authors: musova z. Clin Neurol Neurosurg. 2012 Dec;114(10):1358-60. doi: 10.1016/j.clineuro.2012.03.034. Epub 2012 Apr 11. Clin Neurol Neurosurg. 2012. PMID: 22502787 No abstract available.
CLCN1 mutations in Czech patients with myotonia congenita, in silico analysis of novel and known mutations in the human dimeric skeletal muscle chloride channel.
Skálová D, Zídková J, Voháňka S, Mazanec R, Mušová Z, Vondráček P, Mrázová L, Kraus J, Réblová K, Fajkusová L. Skálová D, et al. Among authors: musova z. PLoS One. 2013 Dec 11;8(12):e82549. doi: 10.1371/journal.pone.0082549. eCollection 2013. PLoS One. 2013. PMID: 24349310 Free PMC article.
19 results