Publication | Closed Access
Recurrent de novo BICD2 mutation associated with arthrogryposis multiplex congenita and bilateral perisylvian polymicrogyria
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Citations
23
References
2016
Year
Mendelian DisorderAutoimmune DiseaseDisease MechanismBilateral Perisylvian PolymicrogyriaGenetic DisorderGeneticsGenetic EpidemiologyPathologyMolecular GeneticsBicd2 MutationMedicineArthrogryposis Multiplex Congenita
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