Molecular analysis of theSMNandNAIPgenes in Iranian spinal muscular atrophy patients-Reference-Cited by-同舟云学术

Molecular analysis of theSMNandNAIPgenes in Iranian spinal muscular atrophy patients

Published:2009-04 Issue:2 Volume:51 Page:193-196
ISSN:1328-8067
Container-title:Pediatrics International
language:en
Short-container-title:

Author:

Omrani Omid,Bonyadi Morteza,Barzgar Mohammad

Publisher

Wiley

Subject

Pediatrics, Perinatology, and Child Health

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1442-200X.2008.02665.x/fullpdf

Reference31 articles.

1. 59th ENMC International Workshop: Spinal Muscular Atrophies: recent progress and revised diagnostic criteria 17-19 April 1998, Soestduinen, The Netherlands;Zerres;Neuromuscul. Disord

2. Prevalence of SMN1 deletion and duplication in carrier and normal populations: Implication for genetic counselling;Cusin;J. Med. Genet,2003

3. Genetic mapping of chronic childhood onset spinal muscular atrophy to chromosome 5q11.2-q13.3;Brzustowicz;Nature,1990

4. Genetic homogeneity between acute and chronic forms of spinal muscular atrophy;Gilliam;Nature,1990

5. Gene for chronic proximal spinal muscular atrophies maps to chromosome 5q;Melki;Nature,1990

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3. A comprehensive overview of SMN and NAIP copy numbers in Iranian SMA patients;Scientific Reports;2023-02-24

4. MLPA analysis for molecular diagnosis of spinal muscular atrophy and correlation of 5q13.2 genes with disease phenotype in Egyptian patients;Egyptian Journal of Medical Human Genetics;2022-12-05

5. Clinical phenotypes of spinal muscular atrophy patients with hybrid SMN gene;Brain and Development;2021-02