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Article

Congenital-onset spastic paraplegia in a patient with TUBB4A mutation and mild hypomyelination.

Journal of the neurological sciences - 15 Sept 2016

Nicita Francesco, Bertini Enrico, Travaglini Lorena, Armando Michelina, Aiello Chiara

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 27538619
DOI: 10.1016/j.jns.2016.07.002

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Congenital-onset spastic paraplegia in a patient with TUBB4A mutation and mild hypomyelination.PMID 27538619Read ↗

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Clinical and genetic characterization of AP4B1-associated SPG47.Semantic proximity Read ↗

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Novel SPG11 Mutation in Hereditary Spastic Paraplegia with Thin Corpus Callosum.Semantic proximity Read ↗

Acquisition of Developmental Milestones in Hypomyelination With Atrophy of the Basal Ganglia and Cerebellum and Other TUBB4A-Related Leukoencephalopathy.Semantic proximity Read ↗

Update on the Genetics of Spastic ParaplegiasSemantic proximity Read ↗

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