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Gene expression profiling in a VRK1 R358X homozygote patient

ABSTRACT: VRK1 mutations in humans cause a severe neuronal phenotype includung spinal muscular atrophy (SMA) and microcephaly. To study the effect of VRK1 R358X mutation on global gene expression in a homozygote human patient, an expression array was performed using EBV-trasformed B cells from the patient and two healthy controls

ORGANISM(S): Homo sapiens

PROVIDER: GSE66061 | GEO | 2015/02/19

SECONDARY ACCESSION(S): PRJNA275793

REPOSITORIES: GEO

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Gene expression profiling in a VRK1 R358X homozygote patient

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