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TUBB4A novel mutation reinforces the genotype-phenotype correlation of hypomyelination with atrophy of the basal ganglia and cerebellum
Letter/Communication   Open access

TUBB4A novel mutation reinforces the genotype-phenotype correlation of hypomyelination with atrophy of the basal ganglia and cerebellum

Daniel Carvalho, Savana Santos, Bernardo Martins and Fernanda Pinto Marques
Brain (London, England : 1878), Vol.138(Pt 2), 327
02/2015
DOI: 10.1093/brain/awu242
PMID: 25168210
url
https://doi.org/10.1093/brain/awu242View
Published (Version of record) Open Access

Abstract

Basal Ganglia - pathology Cerebellum - pathology Female Humans Leukoencephalopathies - pathology Male Mutation - genetics Tubulin - genetics

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