Biallelic variants in TSPOAP1, encoding the active-zone protein RIMBP1, cause autosomal recessive dystonia

Dystonia is a debilitating hyperkinetic movement disorder, which can be transmitted as a monogenic trait. Here, we describe homozygous frameshift, nonsense, and missense variants in TSPOAP1, which encodes the active-zone RIM-binding protein 1 (RIMBP1), as a genetic cause of autosomal recessive dysto...

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Veröffentlicht in:The Journal of clinical investigation 2021-04, Vol.131 (7), p.1-14
Hauptverfasser: Mencacci, Niccolò E, Brockmann, Marisa M, Dai, Jinye, Pajusalu, Sander, Atasu, Burcu, Campos, Joaquin, Pino, Gabriela, Gonzalez-Latapi, Paulina, Patzke, Christopher, Schwake, Michael, Tucci, Arianna, Pittman, Alan, Simon-Sanchez, Javier, Carvill, Gemma L, Balint, Bettina, Wiethoff, Sarah, Warner, Thomas T, Papandreou, Apostolos, Soo, Audrey, Rein, Reet, Kadastik-Eerme, Liis, Puusepp, Sanna, Reinson, Karit, Tomberg, Tiiu, Hanagasi, Hasmet, Gasser, Thomas, Bhatia, Kailash P, Kurian, Manju A, Lohmann, Ebba, Õunap, Katrin, Rosenmund, Christian, Südhof, Thomas C, Wood, Nicholas W, Krainc, Dimitri, Acuna, Claudio
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