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Publications by Dillon Y Chen
Novel KRIT1/CCM1 Heterozygous Nonsense Mutation (C.715 C>T) Associated With Cerebral and Cerebellar Cavernous Malformations in a Paediatric Patient
BMJ Case Reports
Medicine
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Novel KRIT1/CCM1 and MGC4607/CCM2 Gene Variants in Chinese Families With Cerebral Cavernous Malformations
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Loss of P53 Sensitizes Mice With a Mutation in Ccm1 (KRIT1) to Development of Cerebral Vascular Malformations
American Journal of Pathology
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Cerebellar Cavernous Malformations With and Without Associated Developmental Venous Anomalies
BMC Neurology
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Unintentional Drowning Associated With Multiple Cerebral Cavernous Malformations
American Journal of Medical Case Reports
Dysfibrinogenaemia Associated With a Novel Heterozygous Mutation in FGB (C.680delG) and a Mild Clinical History of Bleeding
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Intermediate McAd Deficiency Associated With a Novel Mutation of theACADMGene: C.1052C>T
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Structural Basis for the Disruption of the Cerebral Cavernous Malformations 2 (CCM2) Interaction With Krev Interaction Trapped 1 (KRIT1) by Disease-Associated Mutations
Journal of Biological Chemistry
Biochemistry
Cell Biology
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Ccm3, a Gene Associated With Cerebral Cavernous Malformations, Is Required for Neuronal Migration
Development (Cambridge)
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Arquivos de Neuro-Psiquiatria
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