Detection of deletions and duplications in the Duchenne muscular dystrophy gene by the molecular method MLPA in the first Argentine affected families-Reference-Cited by-同舟云学术

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Detection of deletions and duplications in the Duchenne muscular dystrophy gene by the molecular method MLPA in the first Argentine affected families

Published:2008 Issue:1 Volume:7 Page:223-233
ISSN:1676-5680
Container-title:Genetics and Molecular Research
language:
Short-container-title:Genet. Mol. Res.

Author:

Marzese D.M.,Mampel A.,Gomez L.C.,Echeverria M.I.,Vargas A.L.,Ferreiro V.,Giliberto F.,Roqueì M.

Publisher

Genetics and Molecular Research

Subject

Genetics,Molecular Biology,General Medicine

Link

http://www.funpecrp.com.br/gmr/year2008/vol7-1/pdf/gmr409.pdf

Cited by 6 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. The impact of paralog genes: detection of copy number variation in spinal muscle atrophy patients;BIOCELL;2018

2. Molecular diagnosis of dystrophinopathies using a multi-technique analysis algorithm;Muscle & Nerve;2013-06-26

3. Current mutation discovery approaches in Retinitis Pigmentosa;Vision Research;2012-12

4. Deleción de los genes LIS1, ASPA, TRPV1 y CAMTA2 de la región 17p13.3 en un paciente con síndrome de Miller-Dieker;Revista de Neurología;2011

5. Identification of deletions and duplications in the Duchenne muscular dystrophy gene and female carrier status in western India using combined methods of multiplex polymerase chain reaction and multiplex ligation-dependent probe amplification;Neurology India;2011

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