Expert panel curation of 31 genes in relation to limb girdle muscular dystrophy.
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| Title: | Expert panel curation of 31 genes in relation to limb girdle muscular dystrophy. |
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| Authors: | Mohan S; Department of Genetics, University of North Carolina, Chapel Hill, North Carolina, USA., McNulty S; Department of Genetics, University of North Carolina, Chapel Hill, North Carolina, USA., Thaxton C; Department of Genetics, University of North Carolina, Chapel Hill, North Carolina, USA., Elnagheeb M; Department of Genetics, University of North Carolina, Chapel Hill, North Carolina, USA., Owens E; Department of Genetics, University of North Carolina, Chapel Hill, North Carolina, USA., Flowers M; Department of Genetics, University of North Carolina, Chapel Hill, North Carolina, USA., Nunnery T; Department of Genetics, University of North Carolina, Chapel Hill, North Carolina, USA., Self A; Department of Genetics, University of North Carolina, Chapel Hill, North Carolina, USA., Palus B; Department of Genetics, University of North Carolina, Chapel Hill, North Carolina, USA., Gorokhova S; Aix Marseille Univ, INSERM, MMG, U 1251, Marseille, France.; Department of Medical Genetics, Timone Children's Hospital, APHM, Marseille, France., Kennedy A; Division of Clinical Pharmacology and Toxicology, The Hospital for Sick Children, Toronto, Ontario, Canada., Niu Z; Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota, USA., Johari M; Harry Perkins Institute of Medical Research, Centre for Medical Research, University of Western Australia, Nedlands, Western Australia, Australia.; Folkhälsan Research Center, Department of Medical and Clinical Genetics, Medicum, University of Helsinki, Helsinki, Finland., Maiga AB; Department of Medicine, University of Sciences, Techniques and Technologies of Bamako, Bamako, Mali., Macalalad K; Department of Neurology, Washington University School of Medicine in St. Louis, St Louis, Missouri, USA., Clause AR; Department of Neurology, Washington University School of Medicine in St. Louis, St Louis, Missouri, USA., Beckmann JS; Department of Medical Genetics, University of Lausanne, Lausanne, Switzerland., Bronicki L; Department of clinical genetics, Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada., Cooper ST; Kids Neuroscience Centre, Children's Hospital at Westmead, Westmead, New South Wales, Australia.; School of Medical Sciences, Faculty of Medicine and Health, The University of Sydney, Westmead, New South Wales, Australia.; Functional Neuromics, Children's Medical Research Institute, Westmead, New South Wales, Australia., Ganesh VS; Center for Mendelian Genomics, Broad Institute of MIT and Harvard, Cambridge, Massachusetts, USA.; Department of Neurology, Brigham and Women's Hospital, Boston, Massachusetts, USA., Kang PB; Greg Marzolf Jr. Muscular Dystrophy Center and Department of Neurology, University of Minnesota, Minneapolis, Minnesota, USA., Kesari A; Illumina Inc, San Diego, California, USA., Lek M; Department of Genetics, Yale University School of Medicine, New Haven, Connecticut, USA., Levy J; Coalition to Cure Calpain 3, Westport, Connecticut, USA., Rufibach L; Jain Foundation, Seattle, Washington, USA., Savarese M; Folkhälsan Research Center, Department of Medical and Clinical Genetics, Medicum, University of Helsinki, Helsinki, Finland., Spencer MJ; Department of Neurology, David Geffen School of Medicine at UCLA, Los Angeles, California, USA., Straub V; John Walton Muscular Dystrophy Research Centre, Newcastle University and Newcastle Hospitals NHS Foundation Trusts, Newcastle Upon Tyne, UK., Tasca G; John Walton Muscular Dystrophy Research Centre, Newcastle University and Newcastle Hospitals NHS Foundation Trusts, Newcastle Upon Tyne, UK., Weihl CC; Department of Neurology, Washington University School of Medicine in St. Louis, St Louis, Missouri, USA. |
| Source: | Annals of clinical and translational neurology [Ann Clin Transl Neurol] 2024 Sep; Vol. 11 (9), pp. 2268-2276. Date of Electronic Publication: 2024 Aug 30. |
| Publication Type: | Journal Article |
| Journal Info: | Publisher: Wiley Periodicals, Inc on behalf of American Neurological Association Country of Publication: United States NLM ID: 101623278 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 2328-9503 (Electronic) Linking ISSN: 23289503 NLM ISO Abbreviation: Ann Clin Transl Neurol Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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