المؤلفون: Lucia Daxinger, Maria Iascone, Fred H. Rodriguez, Monique M van Oostaijen-Ten Dam, Ivan K. Chinn, Julio C Orellana, Rocco Piazza, Sonia Bonanomi, Daniele Moratto, Zeynep H. Coban-Akdemir, Wilma G. M. Kroes, Jaime Vengoechea, Manuel Quadri, Claire Booth, Valentina Jarur-Chamy, Frank Baas, Serena Gasperini, Grazia Fazio, Andrea Biondi, Loreani P Noguera, James R. Lupski, Maja Vukic, Gianni Cazzaniga, Giuseppe Gaipa, Francesco Saettini, Raffaele Badolato, Cecilia Poli, Mario Mauri, Marissa R. Shams, Elizabeth Rivers, Cristina Bugarin, Bo Yuan, Amairelys Barroeta Seijas, Silvère M. van der Maarel

المساهمون: Saettini, F, Poli, C, Vengoechea, J, Bonanomi, S, Orellana, J, Fazio, G, Rodriguez III, F, Noguera, L, Booth, C, Jarur-Chamy, V, Shams, M, Iascone, M, Vukic, M, Gasperini, S, Quadri, M, Seijas, A, Rivers, E, Mauri, M, Badolato, R, Cazzaniga, G, Bugarin, C, Gaipa, G, Kroes, W, Moratto, D, van Oostaijen-Ten Dam, M, Baas, F, van der Maarel, S, Piazza, R, Coban-Akdemir, Z, Lupski, J, Yuan, B, Chinn, I, Daxinger, L, Biondi, A

المصدر: Blood
Blood, 137(4), 493-499. AMER SOC HEMATOLOGY

مصطلحات موضوعية: business.industry, Immunology, Hypertrophic cardiomyopathy, Cardiomyopathy, Cell Biology, Hematology, Consanguinity, Neutropenia, medicine.disease, Biochemistry, Phenotype, Uniparental disomy, Agammaglobulinemia, recurrent infections, hypertrophic cardiomyopathy, gene variant, FNIP1, medicine, business, PI3K/AKT/mTOR pathway, Exome sequencing

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::00d8309ae1906c292dfeed4dba4e0454
http://hdl.handle.net/10281/301708