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Phd for Congenital Myasthenic Syndrome (CMS22) and Prader-Willi Syndrome (PWS)

KU LEUVEN | Belgium | 2 months ago

BAP-2026-481 Is the Job related to staff position within a Research Infrastructure? No Offer Description Inactivation of the Prolyl Endopeptidase-Like (PREPL) gene on chromosome 2p21 causes a recessive

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