SPG11: clinical and genetic features of seven Czech patients and literature review-Reference-Cited by-同舟云学术

SPG11: clinical and genetic features of seven Czech patients and literature review

Published:2022-03-07 Issue:5 Volume:44 Page:379-389
ISSN:0161-6412
Container-title:Neurological Research
language:en
Short-container-title:Neurological Research

Author:

Doleckova Kristyna¹,Roth Jan¹,Stellmachova Julia²,Gescheidt Tomas³,Sigut Vladimir⁴,Houska Pavel⁵,Jech Robert¹,Zech Michael⁶⁷,Vyhnalek Martin⁸,Vyhnalkova Emilie⁹,Seeman Pavel¹⁰,Meszarosova Anna Uhrova¹⁰

Affiliation:

1. Department of Neurology and Center of Clinical Neuroscience First Faculty of Medicine, Charles University and General University Hospital in Prague, Prague

2. Department of Medical Genetics, University Hospital Olomouc, Olomouc, Czechia

3. Department of Neurology, St. Anne´s University Hospital, Brno, Czechia

4. Department of Neurology, Krnov Hospital, Krnov

5. Department of Neurology, Strakonice Hospital, Strakonice, Czechia

6. Institute of Neurogenomics, Helmholtz Zentrum München, Munich, Germany

7. Institute of Human Genetics, Technical University of Munich, Munich, Germany

8. Department of Neurology, Second Faculty of Medicine, Charles University and University Hospital Motol, Prague

9. Department of Biology and Medical Genetics, Second Faculty of Medicine, Charles University and University Hospital Motol, Prague

10. Department of Paediatric Neurology, Neurogenetic Laboratory, Second Faculty of Medicine, Charles University and University Hospital Motol, Prague

Funder

European Joint Programme on Rare Diseases

Ministerstvo Zdravotnictví Ceské Republiky