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Paper Details

Whole genome sequencing identifies candidate genes for familial essential tremor and reveals biological pathways implicated in essential tremor aetiology.
EBioMedicine
4
2022
13q21, 16p13, 17q21.31, 21q21.3, 4q13, 4q21, 8q13, AKT, AKT serine/threonine kinase 1, ARL17A, BLK, BTC, CCDC94, EGFR, ENST00000547372, ENST00000547372;, ERK, ET, ET candidate genes, ETS2, EYA1, Essential tremor, G, MAPT, N6AMT1, NPY4R, PCDH9, PDPR, PI3K, PZP, RBFOX1, RNA, SCARB2, SPATA21, SPINK5, STEAP1B, TBC1D3C, TUBB2A, VPS33B, WGS, ZNF736, ZRANB1, bilateral kinetic tremor of the arms, c.4-2A, cancer, candidate genes, chromosome 16p13, collapsed, epidermal growth factor receptor-phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha, essential tremor, exon 2, familial essential tremor, gamma-aminobutyric acid, gene regions, haplotype, neurological disease, neurological disorders, oxygen, patients, phosphatidylinositol-4,5-bisphosphate, protein Kinase 1, rare variants, serine, threonine, tremor
Author NameAffiliation
Gao WangVagelos College of Physicians and Surgeons, Columbia University Irving Medical Center, USA The Center for Statistical Genetics
Allison E Ashley-KochDuke Molecular Physiology Institute, Duke University Medical Center
Suzanne M LealThe Taub Institute for Research on Alzheimer's Disease and The Aging Brain, Columbia University Irving Medical Center, Vagelos College of Physicians and Surgeons, USA The Center for Statistical Genetics
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