Point mutations and a large intragenic deletion in SPG11 in complicated spastic paraplegia without thin corpus callosum-Reference-Cited by-同舟云学术

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Point mutations and a large intragenic deletion in SPG11 in complicated spastic paraplegia without thin corpus callosum

Published:2009-02-05 Issue:5 Volume:46 Page:345-351
ISSN:0022-2593
Container-title:Journal of Medical Genetics
language:en
Short-container-title:Journal of Medical Genetics

Author:

Crimella C,Arnoldi A,Crippa F,Mostacciuolo M L,Boaretto F,Sironi M,D'Angelo M G.,Manzoni S,Piccinini L,Turconi A C,Toscano A,Musumeci O,Benedetti S,Fazio R,Bresolin N,Daga A,Martinuzzi A,Bassi M T

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Cited by 27 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. Identification and analyses of exonic and copy number variants in spastic paraplegia;Scientific Reports;2024-06-21

2. Pluripotent Stem Cells as a Preclinical Cellular Model for Studying Hereditary Spastic Paraplegias;International Journal of Molecular Sciences;2024-02-23

3. Hereditary Spastic Paraplegia Type 11—Clinical, Genetic and Neuroimaging Characteristics;International Journal of Molecular Sciences;2023-12-15

4. Clinical analysis in patients with SPG11 hereditary spastic paraplegia;Frontiers in Neurology;2023-06-15

5. Entropy and Variability: A Second Opinion by Deep Learning;Biomolecules;2022-11-23

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