Trisomy X syndrome with dystonia and a pathogenic SATB1 variant

Ján Necpál; Michael Zech; Juliane Winkelmann; Robert Jech

doi:10.1007/s10072-021-05320-0

Trisomy X syndrome with dystonia and a pathogenic SATB1 variant

Ján Necpál
, Michael Zech
, Juliane Winkelmann
, Robert Jech

Chair of Neurogenetics (2015 — 2023)

Zvolen Hospital
Helmholtz Zentrum München German Research Center for Environmental Health
Technical University of Munich
SyNergy
Charles University

Research output: Contribution to journal › Letter › peer-review

2 Scopus citations

Original language	English
Pages (from-to)	3883-3884
Number of pages	2
Journal	Neurological Sciences
Volume	42
Issue number	9
DOIs	https://doi.org/10.1007/s10072-021-05320-0
State	Published - Sep 2021

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10.1007/s10072-021-05320-0

Cite this

@article{c9fa5c1cf5dd4cb5a6cfeaecc3cff120,

title = "Trisomy X syndrome with dystonia and a pathogenic SATB1 variant",

author = "J{\'a}n Necp{\'a}l and Michael Zech and Juliane Winkelmann and Robert Jech",

note = "Funding Information: This study was co-funded by the Czech Ministry of Health (grant: AZV: NV19-04-00233), by Charles University, Prague, Czech Republic (project: PROGRES Q27), under the frame of the European Joint Programme on Rare Diseases (EJP RD COFUND-EJP N° 825575), and by in-house institutional funding from Technische Universit{\"a}t M{\H u}nchen, Munich, Germany, and Helmholtz Zentrum M{\H u}nchen, Munich, Germany. MZ and JW receive research support from the German Research Foundation (DFG; ZE 1213/2-1; WI 1820/14-1). ",

year = "2021",

month = sep,

doi = "10.1007/s10072-021-05320-0",

language = "English",

volume = "42",

pages = "3883--3884",

journal = "Neurological Sciences",

issn = "1590-1874",

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}

TY - JOUR

T1 - Trisomy X syndrome with dystonia and a pathogenic SATB1 variant

AU - Necpál, Ján

AU - Zech, Michael

AU - Winkelmann, Juliane

AU - Jech, Robert

N1 - Funding Information: This study was co-funded by the Czech Ministry of Health (grant: AZV: NV19-04-00233), by Charles University, Prague, Czech Republic (project: PROGRES Q27), under the frame of the European Joint Programme on Rare Diseases (EJP RD COFUND-EJP N° 825575), and by in-house institutional funding from Technische Universität Műnchen, Munich, Germany, and Helmholtz Zentrum Műnchen, Munich, Germany. MZ and JW receive research support from the German Research Foundation (DFG; ZE 1213/2-1; WI 1820/14-1).

PY - 2021/9

Y1 - 2021/9

UR - https://www.scopus.com/pages/publications/85106422870

U2 - 10.1007/s10072-021-05320-0

DO - 10.1007/s10072-021-05320-0

M3 - Letter

C2 - 34031799

AN - SCOPUS:85106422870

SN - 1590-1874

VL - 42

SP - 3883

EP - 3884

JO - Neurological Sciences

JF - Neurological Sciences

IS - 9

ER -

Trisomy X syndrome with dystonia and a pathogenic SATB1 variant

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