Literature DB >> 25614026

A novel TUBB4A mutation suggests that genotype-phenotype correlation of H-ABC syndrome needs to be revisited.

Roberto Erro1, Joshua Hersheson2, Henry Houlden2, Kailash P Bhatia3.   

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Year:  2015        PMID： 25614026     DOI： 10.1093/brain/awu403

Source DB:  PubMed          Journal:  Brain        ISSN： 0006-8950            Impact factor:   13.501


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  1 in total

1.  Hypomyelination with Atrophy of the Basal Ganglia and Cerebellum (H-ABC) is a Differential Diagnosis for Pallidopyramidal Syndromes with Thin Corpus Callosum.

Authors:  Florian Brugger; Bettina Balint; Elena Antelmi; Kailash P Bhatia
Journal:  Mov Disord Clin Pract       Date:  2016-05-06
  1 in total

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