Genotype–Phenotype Correlations in Iranian Myotonic Dystrophy Type I Patients
Objectives: Myotonic Dystrophy type I (DM1) is a dominantly inherited disorder with a multisystemic pattern affecting skeletal muscle, heart, eye, endocrine and central nervous system. DM1 is associated with the expansion and instability of CTG repeat in the 3' untranslated region of the myoton...
Main Authors: | Kimia Kahrizi, Neda Moradin, Mojtaba Azimian, Bahareh Shojasaffar, Kaveh Alavi, Shahriar Nafisi, Mandana Hasanzad, Seyed Mohammad Ebrahim Moosavi, Azadeh Shirazian, Hossein Najmabadi |
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Format: | Article |
Language: | English |
Published: |
Negah Institute for Scientific Communication
2010-04-01
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Series: | Iranian Rehabilitation Journal |
Subjects: | |
Online Access: | http://irj.uswr.ac.ir/browse.php?a_code=A-10-1-33&slc_lang=en&sid=1 |
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