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De Novo mutations in the β‐tubulin gene TUBB4: From DYT4 to leukoencephalopathy with hypomyelination with atrophy of the basal ganglia and cerebellum (H‐ABC syndrome)
Author(s) -
Alexoudi Athanasia,
Schneider Susanne A.
Publication year - 2013
Publication title -
movement disorders
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.352
H-Index - 198
eISSN - 1531-8257
pISSN - 0885-3185
DOI - 10.1002/mds.25565
Subject(s) - neurology , corticobasal degeneration , atrophy , medicine , neuroscience , pathology , psychology , progressive supranuclear palsy