Genotype–Phenotype Correlations in Iranian Myotonic Dystrophy Type I Patients

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...

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Bibliographic Details
Main Authors: Kimia Kahrizi, Neda Moradin, Mojtaba Azimian, Bahareh Shojasaffar, Kaveh Alavi, Shahriar Nafisi, Mandana Hasanzad, Seyed Mohammad Ebrahim Moosavi, Azadeh Shirazian, Hossein Najmabadi
Format: Article
Language:English
Published: Negah Institute for Scientific Communication 2010-04-01
Series:Iranian Rehabilitation Journal
Subjects:
CTG repeat expansion
Iran
MDRS
Myotonic dystrophy
SSS
Online Access:http://irj.uswr.ac.ir/browse.php?a_code=A-10-1-33&slc_lang=en&sid=1

Internet

http://irj.uswr.ac.ir/browse.php?a_code=A-10-1-33&slc_lang=en&sid=1

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