Multisystem disorder and limb girdle muscular dystrophy caused by LMNA p.R28W mutation.

Türk, Matthias; Wehnert, Manfred; Schröder, Rolf; Chevessier, Frédéric

Türk, Matthias; Wehnert, Manfred; Schröder, Rolf; Chevessier, Frédéric.

Affiliation

Türk M; Department of Neurology, University of Erlangen, Schwabachanlage 6, 91054 Erlangen, Germany.

Neuromuscul Disord ; 23(7): 587-90, 2013 Jul.

Article in En | MEDLINE | ID: mdl-23746545

Subject(s)

Lamin Type A/genetics; Muscular Dystrophies, Limb-Girdle/genetics; Mutation/genetics; Arrhythmias, Cardiac/genetics; Brugada Syndrome; Cardiac Conduction System Disease; Female; Genetic Predisposition to Disease; Heart Conduction System/abnormalities; Heterozygote; Humans; Metabolic Syndrome/complications; Middle Aged; Muscular Dystrophies, Limb-Girdle/complications; Muscular Dystrophies, Limb-Girdle/diagnosis; Phenotype; Young Adult

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Full text: 1 Database: MEDLINE Main subject: Lamin Type A / Muscular Dystrophies, Limb-Girdle / Mutation Type of study: Diagnostic_studies Limits: Adult / Female / Humans / Middle aged Language: En Journal: Neuromuscul Disord Journal subject: NEUROLOGIA Year: 2013 Type: Article Affiliation country: Germany

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