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Autori: Weisburd Ben

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Naslov Diagnosing missed cases of spinal muscular atrophy in genome, exome, and panel sequencing data sets (Article)
Autori Weisburd Ben  ...  Peric Stojan Z  ...  (broj koautora 39) 
Info GENETICS IN MEDICINE, (2025), vol. 27 br. 4, str. -
Projekat European Commission [950-232279]; Canada Research Coordinating Com-mittee New Frontiers in Research Fund [101080249]; Government of Canada, Canada First Research Excellence Fund (CFREF) [NFRFG-2022-00033]; Canadian Institute of Health Research (CIHR) [CFREF-2022-00007]; Wellcome Discovery Award [202210MFE-491707-404816]; Medical Research Council (UK) [226653/Z/22/Z]; Ataxia UK [MR/V009346/1]; Muscular Dystrophy UK; LifeArc Centre to Treat Mitochondrial Diseases (LAC-TreatMito); UKRI/Hori-zon Europe MSCA Doctoral Network Programme [101120256-MMM]; Medical Research Council (MRC); National Institute for Health and Care Research (NIHR) Cambridge Biomedical Research Centre [MR/S005021/1]; Sanofi Genzyme [BRC-1215-20014]; Ultragenyx, LGMD2I Research Fund; LGMD2D Foundation; Kurt+Peter Foundation
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