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S178: A NEW HEREDITARY SYNDROME WITH SEVERE NEUTROPENIA AND NEUROLOGICAL INVOLVEMENT CAUSED BY THE AUTOSOMAL RECESSIVE COPZ1 MUTATION by Natalia Borbaran Bravo, Larissa Doll, Ekaterina Deordieva, Sandro Bräuning, Benjamin Dannenmann, Mohammad Elgamacy, Viktoria Zakharova, Claudia Lengerke, Cornelia Zeidler, Karl Welte, Anna Shcherbina, Julia Skokowa, Maksim Klimiankou
Published 2023-08-01
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