Deletion and duplication mutations spectrum in Duchenne muscular dystrophy in the southwest of Iran

Author:

Shariati Gholamreza,Shakerian Siavash,Mohammadi Anaie Marzieh,Abdorasouli Nehzat,Nanvazadeh Fateme,Sedaghat Alireza,Sedighi Mostafa,Saberi AlihosseinORCID

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference31 articles.

1. Exon deletion pattern in duchene muscular dystrophy in north west of Iran;Barzegar;Iran. J. Child Neurol.,2015

2. Drug treatment of Duchenne muscular dystrophy: available evidence and perspectives;Beytía Mde;Acta Myol.,2012

3. The TREAT-NMD DMD global database: analysis of more than 7,000 Duchenne muscular dystrophy mutations;Bladen;Hum. Mutat.,2015

4. Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and pharmacological and psychosocial management;Bushby;Lancet Neurol.,2010

5. Screening of Duchenne muscular dystrophy (DMD) mutations and investigating its mutational mechanism in Chinese patients;Chen;PLoS One,2014

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