| Original language | English |
|---|---|
| Pages (from-to) | 89-91 |
| Number of pages | 3 |
| Journal | Parkinsonism and Related Disorders |
| Volume | 102 |
| DOIs | |
| State | Published - Sep 2022 |
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In: Parkinsonism and Related Disorders, Vol. 102, 09.2022, p. 89-91.
Research output: Contribution to journal › Letter › peer-review
TY - JOUR
T1 - Dystonia as a prominent feature of TCF20-associated neurodevelopmental disorder
T2 - Expanding the phenotype
AU - Svorenova, Tatiana
AU - Romito, Luigi M.
AU - Colangelo, Isabel
AU - Han, Vladimir
AU - Jech, Robert
AU - Prokisch, Holger
AU - Winkelmann, Juliane
AU - Skorvanek, Matej
AU - Garavaglia, Barbara
AU - Zech, Michael
N1 - Funding Information: This work was supported by the Operational Programme Integrated Infrastructure , funded by the ERDF [ITMS2014+: 313011V455 ] to TL, VH and MS. It was also funded by in-house institutional funding from Technische Universität München, Munich, Germany, Helmholtz Zentrum München, Munich, Germany. It was supported by the National Institute for Neurological Research, Czech Republic , Programme EXCELES, ID Project No. LX22NPO5107 - Next Generation EU, by the Charles University: Cooperation Program in Neuroscience and by the Italian Ministry of Health (Ricerca Corrente 2020–2022) and the Mariani Foundation (CM23). JW and MZ received research support from the German Research Foundation [DFG; WI 1820/14-1 ; ZE 1213/2-1 ]. The “Cell line and DNA Bank of Genetic Movement Disorders and Mitochondrial Diseases” of the Telethon Network of Genetic Biobanks (GTB18001) supplied biological specimens. Funding Information: This work was supported by the Operational Programme Integrated Infrastructure, funded by the ERDF [ITMS2014+:313011V455] to TL, VH and MS. It was also funded by in-house institutional funding from Technische Universität München, Munich, Germany, Helmholtz Zentrum München, Munich, Germany. It was supported by the National Institute for Neurological Research, Czech Republic, Programme EXCELES, ID Project No. LX22NPO5107 - Next Generation EU, by the Charles University: Cooperation Program in Neuroscience and by the Italian Ministry of Health (Ricerca Corrente 2020–2022) and the Mariani Foundation (CM23). JW and MZ received research support from the German Research Foundation [DFG; WI 1820/14-1; ZE 1213/2-1]. The “Cell line and DNA Bank of Genetic Movement Disorders and Mitochondrial Diseases” of the Telethon Network of Genetic Biobanks (GTB18001) supplied biological specimens.
PY - 2022/9
Y1 - 2022/9
UR - http://www.scopus.com/inward/record.url?scp=85135897511&partnerID=8YFLogxK
U2 - 10.1016/j.parkreldis.2022.07.026
DO - 10.1016/j.parkreldis.2022.07.026
M3 - Letter
C2 - 35977450
AN - SCOPUS:85135897511
SN - 1353-8020
VL - 102
SP - 89
EP - 91
JO - Parkinsonism and Related Disorders
JF - Parkinsonism and Related Disorders
ER -