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Corpus callosum thinning in autosomal dominant hereditary spastic paraplegia associated with a novel TUBβ4A mutation
Marta Lamartine S Monteiro1, Isabelle Vandernoot2, Laurence Desmyter2
1Centre de Référence Neuromusculaire, Department of Neurology, Cliniques Universitaires de Bruxelles Hôpital Erasme, Université Libre de Bruxelles (ULB), Brussels, Belgium.
Clinical Genetics
|July 29, 2020
Abstract:
Siblings with hereditary spastic paraplegia and corpus callosum thinning associated with a novel TUBβ4A mutation.

