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Researchers identify new mechanism that causes hereditary diseases

Published: February 9, 2023

Researchers from Charité – Universitätsmedizin Berlin, the Max Planck Institute for Molecular Genetics (MPIMG), and the University Hospital Schleswig-Holstein (UKSH) have investigated in detail how BPTA syndrome, an extremely rare hereditary condition, arises.

Source: news-medical.net

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Denise HornDenes HniszHenri NiskanenMartin MensahEmily HendersonInstitute Of Human GeneticsBerlin Institute Of HealthDigital Clinician Scientist ProgramUniversity Hospital Schleswig HolsteinMax Planck Institute For Molecular GeneticsMax Planck InstituteMolecular GeneticsHuman GeneticsBerlin InstituteIndustry FocusMalte SpielmannDevelopmental Disorder