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

Brain. 2015 Aug;138(Pt 8):e371. doi: 10.1093/brain/awu404. Epub 2015 Jan 24.

Authors

Eline M Hamilton¹, Nicole I Wolf¹, Marjo S van der Knaap²

Affiliations

¹ 1 Department of Child Neurology and Neuroscience Campus Amsterdam, VU University Medical Centre, De Boelelaan 1117, 1081 HV Amsterdam, The Netherlands.
² 1 Department of Child Neurology and Neuroscience Campus Amsterdam, VU University Medical Centre, De Boelelaan 1117, 1081 HV Amsterdam, The Netherlands 2 Department of Functional Genomics, VU University, De Boelelaan 1085, 1081 HV Amsterdam, The Netherlands [email protected].

PMID: 25619510
DOI: 10.1093/brain/awu404

No abstract available

Publication types

Letter
Comment

MeSH terms

Basal Ganglia / pathology*
Cerebellum / pathology*
Female
Humans
Leukoencephalopathies / pathology*
Male
Mutation / genetics*
Tubulin / genetics*

Substances

Tubulin