MFSD7c deficiency links FLVCR2 mutations to microcephaly vasculopathy
Mouse and human data tie MFSD7c deficiency to defective CNS angiogenesis, hypoxia, and microcephaly-associated vasculopathy in Fowler syndrome.
From stroke to neurodegeneration — the science and its clinical impact.
From stroke to neurodegeneration — the science and its clinical impact.