Correlation of SMN2, NAIP, p44, H4F5 and Occludin genes copy number with spinal muscular atrophy phenotype in Tunisian patients-Reference-Cited by-同舟云学术

Correlation of SMN2, NAIP, p44, H4F5 and Occludin genes copy number with spinal muscular atrophy phenotype in Tunisian patients

Published:2012-03 Issue:2 Volume:16 Page:167-174
ISSN:1090-3798
Container-title:European Journal of Paediatric Neurology
language:en
Short-container-title:European Journal of Paediatric Neurology

Author:

Amara Abdelbasset,Adala Labiba,Ben Charfeddine Ilhem,Mamaï Ons,Mili Amira,Lazreg Taheni Ben,H’mida Dorra,Amri Fathi,Salem Najla,Boughammura Lamia,Saad Ali,Gribaa Moez

Publisher

Elsevier BV

Subject

Clinical Neurology,General Medicine,Pediatrics, Perinatology, and Child Health

Reference26 articles.

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4. Consensus statement for standard of care in spinal muscular atrophy;Wang;J Child Neurol,2007

5. Structure and organization of the human survival motor neurone (SMN) gene;Burglen;Genomics,1996

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