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Article

Novel FTA2 variants were observed in patients with restless legs syndrome via whole-exome sequencing

2024-04-11

Abstract excerpt

<title>Abstract</title> <p><bold>Background:</bold> Restless legs syndrome (RLS) is often characterized by familial aggregation. Molecular genetic changes are closely related to the occurrence of the disease, but the key gene variations are unclear. Here, genetic changes were investigated in an RLS family. <bold>Methods: </bold>4 ml EDTA anticoagulant peripheral blood was collected from patients in a family with...

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Literature Corpus work
9de3d03d-8d17-5c9c-b2a0-ee648843be39
DOI
10.21203/rs.3.rs-4105454/v1
Open publication

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Novel FTA2 variants were observed in patients with restless legs syndrome via whole-exome sequencingDOI 10.21203/rs.3.rs-4105454/v1
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