Frequency of SMN1 exon 7 deletion in patients with spinal muscular atrophy in Kashmir

Author:

Syed Shafia,Zargar Mahrukh H.,Pandith Arshad,Khan Nabeela,Ahmad Rehana,Mahajan Qurteeba,Qazi Wardha

Funder

Sher-I-Kashmir Institute of Medical Sciences Hospital, Kashmir

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference32 articles.

1. Molecular genetics of spinal muscular atrophy: contribution of the NAIP gene to clinical severity;Akutsu;Kobe J. Med. Sci.,2002

2. Molecular analysis of the SMN and NAIP genes in Saudi spinal muscular atrophy patients;Al Rajeh;J. Neurol. Sci.,1998

3. High incidence of SMN1 gene deletion in Moroccan adult-onset spinal muscular atrophy patients;Bouhouche;J. Neurol.,2003

4. A frame-shift deletion in the survival motor neuron gene in Spanish spinal muscular atrophy patients;Bussaglia;Nat. Genet.,1995

5. Correlation between genotype and phenotype in Korean patients with spinal muscular atrophy;Cho;Mol. Cells,2001

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