Article
Intermittent granulocyte maturation arrest, hypocellular bone marrow, and episodic normal neutrophil count can be associated with SRP54 mutations causing Shwachman-Diamond-like syndrome.
British journal of haematology - 1 May 2020
Saettini Francesco, Cattoni Alessandro, D'Angio' Mariella, Corti Paola, Maitz Silvia, Pagni Fabio, Seminati Davide, Pezzoli Laura, Iascone Maria, Biondi Andrea, Bonanomi Sonia
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