Recurrent de novo BICD2 mutation associated with arthrogryposis multiplex congenita and bilateral perisylvian polymicrogyria

Research output: Contribution to journal › Case report › Contributed › peer-review

Contributors

G. Ravenscroft - (Author)
N. Di Donato - , Institute of Clinical Genetics (Author)
G. Hahn - , Institute and Polyclinic of Diagnostic and Interventional Radiology (Author)
M.R. Davis - (Author)
P.D. Craven - (Author)
G. Poke - (Author)
K.R. Neas - (Author)
T.M. Neuhann - (Author)
W.B. Dobyns - (Author)
N.G. Laing - (Author)

Scopus	84991254153
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