Emery-Dreifuss Muscular Dystrophy: a Report of a Large Family with 11 Affected Individuals

نویسندگان

  • Abbas Tafakhori Department of Neurology, School of Medicine, Imam Khomeini Hospital and Iranian Center of Neurological Research, Tehran University of Medical Sciences, Tehran, Iran.
  • Azadeh Ahmadifard Department of Medical Genetics, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
  • Hossein Darvish Department of Medical Genetics, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
  • Javad Jamshidi Noncommunicable Diseases Research Center, Fasa University of Medical Sciences, Fasa, Iran.
  • Zeinab Falsafi Department of Neurology, School of Medicine, Imam Khomeini Hospital and Iranian Center of Neurological Research, Tehran University of Medical Sciences, Tehran, Iran.
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[Emery-Dreifuss muscular dystrophy].

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[Emery-Dreifuss muscular dystrophy: case report].

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Mutations in genes encoding the nuclear envelope proteins emerin and lamin A/C lead to a range of tissue-specific degenerative diseases. These include dilated cardiomyopathy, limb-girdle muscular dystrophy and X-linked and autosomal dominant EDMD (Emery-Dreifuss muscular dystrophy). The molecular mechanisms underlying these disorders are poorly understood; however, recent work using animal mode...

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عنوان ژورنال

دوره 5  شماره None

صفحات  196- 198

تاریخ انتشار 2016-07

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