Homozygous exon 7 deletion of the SMN centromeric gene (SMN2): A potential susceptibility factor for adult-onset lower motor neuron disease-Reference-Cited by-同舟云学术

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Homozygous exon 7 deletion of the SMN centromeric gene (SMN2): A potential susceptibility factor for adult-onset lower motor neuron disease

Published:2002-03-01 Issue:3 Volume:249 Page:290-293
ISSN:0340-5354
Container-title:Journal of Neurology
language:
Short-container-title:Journal of Neurology

Author:

Echaniz-Laguna Andoni,Guiraud-Chaumeil Christophe,Tranchant Christine,Reeber André,Melki Judith,Warter Jean-Marie

Publisher

Springer Science and Business Media LLC

Subject

Neurology (clinical),Neurology

Link

http://link.springer.com/content/pdf/10.1007/s004150200007.pdf

Cited by 31 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 Spectrum of Childhood-Onset Lower Motor Neuron Disease of Spinal Muscular Atrophy Phenotype Associated with Survival Motor Neuron-2 Gene Deletion;Journal of Pediatric Neurology;2024-07-30

2. Real-Time PCR-Based Screening for Homozygous SMN2 Deletion Using Residual Dried Blood Spots;Genes;2023-11-29

3. Neurogenic Disorders;Muscle Biopsy;2020

4. Discovery of a Small Molecule Probe That Post-Translationally Stabilizes the Survival Motor Neuron Protein for the Treatment of Spinal Muscular Atrophy;Journal of Medicinal Chemistry;2017-05-19

5. Muscle histopathology in today′s era of molecular genetics: Role and limitations;Annals of Indian Academy of Neurology;2015

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