Solving unsolved rare neurological diseases-a Solve-RD viewpoint

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Veröffentlicht in:	European journal of human genetics : EJHG 2021-09, Vol.29 (9), p.1332-1336
Hauptverfasser:	Schuele, Rebecca, Timmann, Dagmar, Erasmus, Corrie E., Reichbauer, Jennifer, Wayand, Melanie, van de Warrenburg, Bart, Schoels, Ludger, Wilke, Carlo, Bevot, Andrea, Zuchner, Stephan, Beltran, Sergi, Laurie, Steven, Matalonga, Leslie, Graessner, Holm, Synofzik, Matthis
Format:	Artikel
Sprache:	eng
Schlagworte:	Ataxia Atrophy Biochemistry & Molecular Biology Consortia Datasets as Topic Disease Genes Genetic Testing - methods Genetic Testing - standards Genetics Genetics & Heredity Genomes Genomics Genomics - methods Genomics - standards Hospitals Human genetics Humans Life Sciences Life Sciences & Biomedicine Nervous System Diseases - genetics Nervous System Diseases - pathology Neurological diseases Neurology Pediatrics Practice Guidelines as Topic Rare Diseases - genetics Rare Diseases - pathology Science & Technology Viewpoint Whole Exome Sequencing - methods Whole Exome Sequencing - standards
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