Literature DB >> 24013879

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).

Athanasia Alexoudi1, Susanne A Schneider.   

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Year:  2013        PMID： 24013879     DOI： 10.1002/mds.25565

Source DB:  PubMed          Journal:  Mov Disord        ISSN： 0885-3185            Impact factor:   10.338


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  1 in total

1.  Acquisition of Developmental Milestones in Hypomyelination With Atrophy of the Basal Ganglia and Cerebellum and Other TUBB4A-Related Leukoencephalopathy.

Authors:  Francesco Gavazzi; Brittany A Charsar; Catherine Williams; Justine Shults; Cesar A Alves; Laura Adang; Adeline Vanderver
Journal:  J Child Neurol       Date:  2021-09       Impact factor: 2.363
  1 in total

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