Vincent Cantagrel
0000-0002-5180-4848
3 papers found
Refreshing results…
Recessive PRDM13 mutations cause fatal perinatal brainstem dysfunction with cerebellar hypoplasia and disrupt Purkinje cell differentiation
Inherited glycosylphosphatidylinositol defects cause the rare Emm-negative blood phenotype and developmental disorders
High N-glycan multiplicity is critical for neuronal adhesion and sensitizes the developing cerebellum to N-glycosylation defect
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