Intermittent granulocyte maturation arrest, hypocellular bone marrow, and episodic normal neutrophil count can be associated with SRP54 mutations causing Shwachman–Diamond-like syndrome
العنوان: | Intermittent granulocyte maturation arrest, hypocellular bone marrow, and episodic normal neutrophil count can be associated with SRP54 mutations causing Shwachman–Diamond-like syndrome |
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المؤلفون: | Fabio Pagni, Maria Iascone, Mariella D'Angiò, Francesco Saettini, Sonia Bonanomi, Davide Seminati, Paola Corti, Laura Pezzoli, Silvia Maitz, Andrea Biondi, Alessandro Cattoni |
المساهمون: | Saettini, F, Cattoni, A, D'Angiò, M, Corti, P, Maitz, S, Pagni, F, Seminati, D, Pezzoli, L, Iascone, M, Biondi, A, Bonanomi, S |
بيانات النشر: | Blackwell Publishing Ltd, 2020. |
سنة النشر: | 2020 |
مصطلحات موضوعية: | Shwachman–Diamond syndrome, Pathology, medicine.medical_specialty, SRP54, Hypocellular Bone Marrow, business.industry, Shwachman-Diamond syndrome, Diamond, Hematology, Granulocyte, engineering.material, medicine.disease, Maturation arrest, medicine.anatomical_structure, severe congenital neutropenia, inborn error of immunity, Absolute neutrophil count, engineering, Medicine, business |
وصف الملف: | ELETTRONICO |
اللغة: | English |
الوصول الحر: | https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa9f63221e0ddf2179e36d9e24a20a4aTest http://hdl.handle.net/10281/271102Test |
حقوق: | OPEN |
رقم الانضمام: | edsair.doi.dedup.....aa9f63221e0ddf2179e36d9e24a20a4a |
قاعدة البيانات: | OpenAIRE |
الوصف غير متاح. |