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)
Mov Disord
.
2013 Sep;28(10):1343.
doi: 10.1002/mds.25565.
Epub 2013 Sep 6.
Authors
Athanasia Alexoudi
1
,
Susanne A Schneider
Affiliation
1
Department of Neurology, University of Kiel, Kiel, Germany.
PMID:
24013879
DOI:
10.1002/mds.25565
No abstract available
Publication types
Comment
MeSH terms
Basal Ganglia / pathology*
Cerebellum / pathology*
Female
Humans
Leukoencephalopathies / genetics*
Male
Models, Molecular*
Protein Conformation*
Tubulin / genetics*
Substances
Tubulin