Publications
Export 2 results:
Author Title [ Year
] Filters: Author is Wiszniewski, Wojciech and Keyword is Magnetic Resonance Imaging [Clear All Filters]
Mutations in VRK1 associated with complex motor and sensory axonal neuropathy plus microcephaly. JAMA Neurol 70, 1491-8 (2013).
TM4SF20 ancestral deletion and susceptibility to a pediatric disorder of early language delay and cerebral white matter hyperintensities. Am J Hum Genet 93, 197-210 (2013).
