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

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 ms.vanderknaap@vumc.nl.

Comment

Eline M Hamilton et al. Brain. 2015 Aug.

. 2015 Aug;138(Pt 8):e371.

doi: 10.1093/brain/awu404. Epub 2015 Jan 24.

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 ms.vanderknaap@vumc.nl.

No abstract available

Comment on

Hypomyelination with atrophy of the basal ganglia and cerebellum: further delineation of the phenotype and genotype-phenotype correlation.
Hamilton EM, Polder E, Vanderver A, Naidu S, Schiffmann R, Fisher K, Raguž AB, Blumkin L; H-ABC Research Group; van Berkel CG, Waisfisz Q, Simons C, Taft RJ, Abbink TE, Wolf NI, van der Knaap MS. Hamilton EM, et al. Brain. 2014 Jul;137(Pt 7):1921-30. doi: 10.1093/brain/awu110. Epub 2014 Apr 30. Brain. 2014. PMID: 24785942 Free PMC article.
A novel TUBB4A mutation suggests that genotype-phenotype correlation of H-ABC syndrome needs to be revisited.
Erro R, Hersheson J, Houlden H, Bhatia KP. Erro R, et al. Brain. 2015 Aug;138(Pt 8):e370. doi: 10.1093/brain/awu403. Epub 2015 Jan 21. Brain. 2015. PMID: 25614026 No abstract available.