Turkish families with juvenile motor neuron disease broaden the phenotypic spectrum ofSPG11-Reference-Cited by-同舟云学术

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Turkish families with juvenile motor neuron disease broaden the phenotypic spectrum ofSPG11

Published:2015-10 Issue:3 Volume:1 Page:e25
ISSN:2376-7839
Container-title:Neurology Genetics
language:en
Short-container-title:Neurol Genet

Author:

Iskender Ceren,Kartal Ece,Akcimen Fulya,Kocoglu Cemile,Ozoguz Aslihan,Kotan Dilcan,Eraksoy Mefkure,Parman Yesim G.,Basak Ayse Nazli

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Genetics(clinical),Clinical Neurology

Reference21 articles.

1. HEREDITARY MOTOR SYSTEM DISEASES (CHRONIC JUVENILE AMYOTROPHIC LATERAL SCLEROSIS)

2. A mutation in sigma-1 receptor causes juvenile amyotrophic lateral sclerosis

3. Linkage of the Gene for an Autosomal Dominant Form of Juvenile Amyotrophic Lateral Sclerosis to Chromosome 9q34

4. Linkage of recessive familial amyotrophic lateral sclerosis to chromosome 2q33–q35

5. Linkage of a commoner form of recessive amyotrophic lateral sclerosis to chromosome 15q15-q22 markers

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

2. Revisiting the complex architecture of ALS in Turkey: Expanding genotypes, shared phenotypes, molecular networks, and a public variant database;Human Mutation;2020-06-24

3. Description of combined ARHSP/JALS phenotype in some patients with SPG11 mutations;Molecular Genetics & Genomic Medicine;2020-05-08

4. Janus-faced spatacsin (SPG11): involvement in neurodevelopment and multisystem neurodegeneration;Brain;2020-05-01

5. Chinese families with autosomal recessive hereditary spastic paraplegia caused by mutations in SPG11;BMC Neurology;2020-01-03

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