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Academic Journal

Diagnostic laboratory testing for Charcot Marie Tooth disease (CMT): the spectrum of gene defects in Norwegian patients with CMT and its implications for future genetic test strategies.

  • Authors : Østern R; Department of Medical Genetics, University Hospital of North-Norway, Tromsø NO9038, Norway. .; Fagerheim T

Subjects: Genetic Testing*; Charcot-Marie-Tooth Disease/Charcot-Marie-Tooth Disease/Charcot-Marie-Tooth Disease/*diagnosis ; White People/White People/White People/*genetics

  • Source: BMC medical genetics [BMC Med Genet] 2013 Sep 21; Vol. 14, pp. 94. Date of Electronic Publication: 2013 Sep 21.Publisher: BioMed Central Country of Publication: England NLM ID: 100968552 Publication Model: Electronic Cited Medium: Internet ISSN: 1471-2350

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Academic Journal

Facioscapulohumeral muscular dystrophy and Charcot-Marie-Tooth neuropathy 1A - evidence for "double trouble" overlapping syndromes.

  • Authors : Schreiber O; Friedrich-Baur-Institute, Department of Neurology, Ludwig-Maximilians-University Munich, Ziemssenstrasse 1, D-80336 Munich, Germany. .; Schneiderat P

Subjects: Charcot-Marie-Tooth Disease/Charcot-Marie-Tooth Disease/Charcot-Marie-Tooth Disease/*genetics ; Muscular Dystrophy, Facioscapulohumeral/Muscular Dystrophy, Facioscapulohumeral/Muscular Dystrophy, Facioscapulohumeral/*genetics; Charcot-Marie-Tooth Disease/Charcot-Marie-Tooth Disease/Charcot-Marie-Tooth Disease/pathology

  • Source: BMC medical genetics [BMC Med Genet] 2013 Sep 16; Vol. 14, pp. 92. Date of Electronic Publication: 2013 Sep 16.Publisher: BioMed Central Country of Publication: England NLM ID: 100968552 Publication Model: Electronic Cited Medium: Internet ISSN: 1471-2350

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  • 1-4 ل  4 نتائج ل ""Myelin Proteins""