L239F founder mutation in GDAP1 is associated with a mild Charcot–Marie–Tooth type 4C4 (CMT4C4) phenotype von Kabzińska, Dagmara, Strugalska-Cynowska, Halina, Kostera-Pruszczyk, Anna, Ryniewicz, Barbara, Posmyk, Renata, Midro, Alina, Seeman, Pavel, Báranková, Lucia, Zimoń, Magdalena, Baets, Jonathan, Timmerman, Vincent, Guergueltcheva, Velina, Tournev, Ivailo, Sarafov, Stayko, De Jonghe, Peter, Jordanova, Albena, Hausmanowa-Petrusewicz, Irena, Kochański, Andrzej

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Mutations in the LMNA gene do not cause axonal CMT in Czech patients von Laššuthová, Petra, Baránková, Lucia, Haberlová, Jana, Mazanec, Radim, Wallace, Andrew, Huehne, Kathrin, Rautenstrauss, Bernd, Seeman, Pavel

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Emery-Dreifuss Muscular Dystrophy: A Novel Mutation in the LMNA Gene von Laššuthová, Petra, MD, Baránková, Lucia, MD, Kraus, Josef, MD, CSc, Maříková, Tat'ána, MD, CSc, Seeman, Pavel, MD, PhD

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Emery-Dreifuss Muscular Dystrophy: A Novel Mutation in the +AEAAQA-iLMNA+AEA- Gene von Lassuthova, Petra, Barankova, Lucia, Kraus, Josef, Marikova, Tat+IBk-ana, Seeman, Pavel

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L239F founder mutation in GDAPI is associated with a mild Charcot-Marie-Tooth type 4C4 (CMT4C4) phenotype von KABZINSKA, Dagmara, STRUGALSKA-CYNOWSKA, Halina, TIMMERMAN, Vincent, GUERGUELTCHEVA, Velina, TOURNEV, Ivailo, SARAFOV, Stayko, DE JONGHE, Peter, JORDANOVA, Albena, HAUSMANOWA-PETRUSEWICZ, Irena, KOCHANSKI, Andrzej, KOSTERA-PRUSZCZYK, Anna, RYNIEWICZ, Barbara, POSMYK, Renata, MIDRO, Alina, SEEMAN, Pavel, BARANKOVA, Lucia, ZIMON, Magdalena, BAETS, Jonathan

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Dědičné ulceromutilující senzitivní neuropatie – klinická, elektrofyziologická a molekulárně genetická studie tří rodin von Šafka-Brožková, Dana, Mazanec, Radim, Böhm, Jiří, Vyšata, Oldřich, Auer-Grumbach, M, Windpassinger, Ch, Neupauerová, Jana, Baránková, Lucia, Nevšímalová, Soňa, Seeman, Pavel

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