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Corpus callosum thinning in autosomal dominant hereditary spastic paraplegia associated with a novel TUBβ4A mutation
Author(s) -
Lamartine S. Monteiro Marta,
Vandernoot Isabelle,
Desmyter Laurence,
Wermenbol Vanessa,
Naeije Gilles,
Remiche Gauthier
Publication year - 2020
Publication title -
clinical genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.543
H-Index - 102
eISSN - 1399-0004
pISSN - 0009-9163
DOI - 10.1111/cge.13809
Subject(s) - hereditary spastic paraplegia , corpus callosum , mutation , spastic , paraplegia , medicine , genetics , phenotype , pathology , biology , physical medicine and rehabilitation , gene , spinal cord , cerebral palsy , psychiatry
Siblings with hereditary spastic paraplegia and corpus callosum thinning associated with a novel TUBβ4A mutation.
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