Intermittent granulocyte maturation arrest, hypocellular bone marrow, and episodic normal neutrophil count can be associated with SRP54 mutations causing Shwachman–Diamond-like syndrome

التفاصيل البيبلوغرافية
العنوان: Intermittent granulocyte maturation arrest, hypocellular bone marrow, and episodic normal neutrophil count can be associated with SRP54 mutations causing Shwachman–Diamond-like syndrome
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