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A heterozygous mutation in the CCDC88C gene likely causes early-onset pure hereditary spastic parapl…
Neuropathological hallmarks of fetal hydrocephalus linked to CCDC88C pathogenic variants.
Beneficial tyrosine kinase inhibitor therapy in a patient with relapsed BCR-ABL1-like acute lymphobl…
Two Isoforms of the Guanine Nucleotide Exchange Factor, Daple/CCDC88C Cooperate as Tumor Suppressors…
CCDC88C-FLT3 gene fusion in CD34-positive haematopoietic stem and multilineage cells in myeloid/lymp…
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Promoting Pupils' Physical Literacy
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