Thinning of the Corpus Callosum and Cerebellar Atrophy is Correlated with Phenotypic Severity in a Family with Spastic Paraplegia Type 11

Eitemau Tebyg

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  Cyhoeddwyd: (2009)
• Clinical Heterogeneity and Genotype Phenotype correlations in Hereditary Spastic Paraplegia (HSP) due to Spatacsin mutations (SPG11)
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• SPG11 mutations are common in familial cases of complicated hereditary spastic paraplegia (HSP)
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• Expanding the Clinical Spectrum of SPG11 Gene Mutations in Recessive Hereditary Spastic Paraplegia with Thin Corpus Callosum
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• Hereditary Spastic Paraplegia with Mental Impairment, Thin Corpus Callosum and Amyotrophy: A Road Map to SPG11 Contributors
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  Cyhoeddwyd: (2020)