The role of PQBP1 in neural development and function.
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DOI: 10.1042/bst20220920
Abstract: Mutations in the polyglutamine tract-binding protein 1 (PQBP1) gene are associated with Renpenning syndrome, which is characterized by microcephaly, intellectual deficiency, short stature, small testes, and distinct facial dysmorphism. Studies using different models have revealed… read more here.
Keywords: neural development; function; role pqbp1; pqbp1 neural ... See more keywords