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Paper Details

Mutations in VRK1 associated with complex motor and sensory axonal neuropathy plus microcephaly.
JAMA Neurol
52
2013
Patients, VRK1, axonal motor and sensory neuropathy, axonal sensorimotor neuropathy, cerebral dysgenesis, children, complex motor and sensory axonal neuropathy, complex neuropathy, haplotype, microcephaly, mutant alleles, neurological diseases, neuropathy, patient, patients, rare, single-nucleotide polymorphism arrays, vaccinia-related kinase 1 gene
Author NameAffiliation
Leila JamalKennedy Krieger Institute
Shalini N JhangianiBaylor College of Medicine
Jeffrey G ReidBaylor College of Medicine
Jeffrey G ReidBaylor College of Medicine
Donna M MuznyBaylor College of Medicine
Donna M MuznyBaylor College of Medicine
Eric BoerwinkleBaylor College of Medicine, Texas6Human Genetics Center and Institute of Molecular Medicine, University of Texas Health Science Center at Houston
Eric BoerwinkleBaylor College of Medicine, Texas6Human Genetics Center and Institute of Molecular Medicine, University of Texas Health Science Center at Houston
James R LupskiBaylor College of Medicine, Texas2Texas Children's Hospital
James R LupskiBaylor College of Medicine, Texas2Texas Children's Hospital
Richard A GibbsBaylor College of Medicine
Richard A GibbsBaylor College of Medicine
Wojciech WiszniewskiBaylor College of Medicine
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