Associated Papers
Spastic paraplegia type 76 due to novel CAPN1 mutations: three case reports with literature review.
Zhu Z et al.
Neurogenetics, 2023
"Ear of the Lynx" Sign in Hereditary Spastic Paraparesis (HSP) 76.
Agarwal A et al.
Movement Disorders Clinical Practice, 2023
CAPN1 and hereditary spastic paraplegia: a novel variant in an Iranian family and overview of the genotype-phenotype correlation.
Rahimi Bidgoli MM et al.
The International Journal of Neuroscience, 2021
Increasing involvement of CAPN1 variants in spastic ataxias and phenotype-genotype correlations.
Méreaux JL et al.
Neurogenetics, 2021
Novel CAPN1 mutations extend the phenotypic heterogeneity in combined spastic paraplegia and ataxia.
Lai LL et al.
Annals of Clinical and Translational Neurology, 2020
CAPN1 mutations: Expanding the CAPN1-related phenotype: From hereditary spastic paraparesis to spastic ataxia.
Shetty A et al.
European Journal of Medical Genetics, 2019
Two novel homozygous mutations of CAPN1 in Chinese patients with hereditary spastic paraplegia and literatures review.
Peng F et al.
Orphanet Journal of Rare Diseases, 2019
A Novel CAPN1 Mutation Causes a Pure Hereditary Spastic Paraplegia in an Italian Family.
Cotti Piccinelli S et al.
Frontiers in Neurology, 2019
CAPN1 Variants as Cause of Hereditary Spastic Paraplegia Type 76.
Garcia-Berlanga JE et al.
Case Reports in Neurological Medicine, 2019
CAPN1 mutations broadening the hereditary spastic paraplegia/spinocerebellar ataxia phenotype.
Lambe J et al.
Practical Neurology, 2018
Defects in the CAPN1 Gene Result in Alterations in Cerebellar Development and Cerebellar Ataxia in Mice and Humans.
Wang Y et al.
Cell Reports, 2016
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