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Autori: Johari Mridul

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Naslov Missense variants in TUBA4A cause myo-tubulinopathies (Article; Early Access)
Autori Johari Mridul  ...  Milic-Rasic Vedrana  Kovacevic Gordana  Kosac Ana  ...  (broj koautora 66) 
Info BRAIN, (2026), vol. br. , str. -
Projekat the Academy of Medical Sciences [APR8\1017]; Italian Ministry of Health [RF-2021-12374963]; Sigrid Juselius Foundation [230217]; Broad Institute of MIT and Harvard [U01HG011755]; NICHD; National Human Genome Research Institute [P50HD105351, UM1 HG008900, U01 HG011755, R01 HG009141, 2022-309464, 2019-199278]; Fred Liuzzi Foundation; National Heart, Lung and Blood Institute; Ultragenyx; National Eye Institute; Samantha J. Brazzo Foundation [101080844, 339434, 346209, 361979, 23281]; Australian Government research training program scholarship; Jean Rogerson HDR Scholarship [BOS1139-1]; Sanofi Genzyme; Association Franaise contre les Myopathies [24438, RPG075-2024, APP2007681, APP2023357]; an Australian NHMRC Fellowship [APP2007769]
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science  
Naslov Deciphering the Genetic Landscape of Unsolved Congenital Myopathies: A Multinational Research Approach (Meeting Abstract)
Autori Johari Mridul  ...  Kovacevic Gordana  ...  Milic Vedrana  ...  (broj koautora 34) 
Info EUROPEAN JOURNAL OF HUMAN GENETICS, (2024), vol. 32 br. , Suppl. 2, str. 844-845
Projekat AFM-Telethon [24438, APP2002640]
Ispravka ISI/Web of Science   Elečas   Rang časopisa  
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