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Novel mutations in the DYNC1H1 tail domain refine the genetic and clinical spectrum of dyneinopathies.
Peeters, Kristien; Bervoets, Sven; Chamova, Teodora; Litvinenko, Ivan; De Vriendt, Els; Bichev, Stoyan; Kancheva, Dahlia; Mitev, Vanyo; Kennerson, Marina; Timmerman, Vincent; De Jonghe, Peter; Tournev, Ivailo; MacMillan, John; Jordanova, Albena.
Affiliation
  • Peeters K; Molecular Neurogenomics Group, Department of Molecular Genetics, VIB, Antwerp, Belgium; Neurogenetics Laboratory, Institute Born-Bunge, University of Antwerp, Antwerp, Belgium.
Hum Mutat ; 36(3): 287-91, 2015 Mar.
Article in En | MEDLINE | ID: mdl-25512093
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Muscular Atrophy, Spinal / Charcot-Marie-Tooth Disease / Dyneins / Cytoplasmic Dyneins / Mutation Type of study: Prognostic_studies Limits: Humans Language: En Journal: Hum Mutat Journal subject: GENETICA MEDICA Year: 2015 Document type: Article Affiliation country: Belgium Country of publication: United States
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Muscular Atrophy, Spinal / Charcot-Marie-Tooth Disease / Dyneins / Cytoplasmic Dyneins / Mutation Type of study: Prognostic_studies Limits: Humans Language: En Journal: Hum Mutat Journal subject: GENETICA MEDICA Year: 2015 Document type: Article Affiliation country: Belgium Country of publication: United States