التشخيص الجزيئى لمرض التوتر العضلى الضمورى فى المرضى المصريين Molecular Diagnosis of Myotonic Dystrophy Type 1 in Egyptian Patients
هدى عبد الله أحمد رضوان Hoda Abdallah Ahmed Radwan;
Abstract
Myotonic dystrophy type 1 (DM1) also called dystrophia myotonica is an autosomal dominant disorder that results from expansion of unstable trinucleotide repeats in the 3'untranslated region of the dystrophia myotonica protein kinase (DMPK) gene. It is the
Other data
| Title | التشخيص الجزيئى لمرض التوتر العضلى الضمورى فى المرضى المصريين Molecular Diagnosis of Myotonic Dystrophy Type 1 in Egyptian Patients | Authors | هدى عبد الله أحمد رضوان Hoda Abdallah Ahmed Radwan | Keywords | التشخيص الجزيئى لمرض التوتر العضلى الضمورى فى المرضى المصريين Molecular Diagnosis of Myotonic Dystrophy Type 1 in Egyptian Patients | Issue Date | 2009 | Description | Myotonic dystrophy type 1 (DM1) also called dystrophia myotonica is an autosomal dominant disorder that results from expansion of unstable trinucleotide repeats in the 3'untranslated region of the dystrophia myotonica protein kinase (DMPK) gene. It is the |
Attached Files
| File | Size | Format | |
|---|---|---|---|
| Binder1.pdf | 305.26 kB | Adobe PDF | View/Open |
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