Erratum to: Biallelic variants in HPDL cause pure and complicated hereditary spastic paraplegia
Author(s) -
Manuela Wiessner,
Reza Maroofian,
Meng-Yuan Ni,
Andrea Pedroni,
Juliane Müller,
Rolf Stucka,
Christian Beetz,
Stéphanie Efthymiou,
Filippo M. Santorelli,
Ahmed Alfares,
Changlian Zhu,
Anna Uhrová Mészárosová,
Elham Alehabib,
Somayeh Bakhtiari,
Andreas Janecke,
María Gabriela Otero,
Jin Yun Helen Chen,
James Peterson,
Tim M. Strom,
Peter De Jonghe,
Tine Deconinck,
Willem De Ridder,
Jonathan De Winter,
Rossella Pasquariello,
Ivana Ricca,
Majid Alfadhel,
Bart P.C. van de Warrenburg,
R Portier,
Carsten Bergmann,
Saghar Ghasemi Firouzabadi,
Sheng Chih Jin,
Kaya Bilgüvar,
Sherifa A. Hamed,
Mohammed Abdelhameed,
Nourelhoda A. Haridy,
Shazia Maqbool,
Fatima Rahman,
Najwa Anwar,
Jenny Carmichael,
Alistair T. Pagnamenta,
Nicholas Wood,
Frédéric Tran MauThem,
Tobias B. Haack,
Maja Di Rocco,
Isabella Ceccherini,
Michele Iacomino,
Federico Zara,
Vincenzo Salpietro,
Marcello Scala,
Marta Rusmini,
Yiran Xu,
Yinghong Wang,
Yasuhíro Suzuki,
Kishin Koh,
Haitian Nan,
Hiroyuki Ishiura,
Shoji Tsuji,
Laëtitia Lambert,
Emmanuelle Schmitt,
Elodie Lacaze,
Hanna Küpper,
David Dredge,
Cara Skraban,
Amy B. Goldstein,
Mary Willis,
Katheryn Grand,
John M. Graham,
Richard A. Lewis,
Francisca Millan,
Özgür Duman,
Nihal Olgaç Dündar,
Gökhan Uyanık,
Lüdger Schöls,
Peter Nürnberg,
Gudrun Nürnberg,
Andrea Català-Bordes,
Pavel Seeman,
Martin Kuchar,
Hossein Darvish,
Adriana Rebelo,
Filipa Bouçanova,
JeanJacques Médard,
Roman Chrast,
Michaela AuerGrumbach,
Fowzan S. Alkuraya,
Hanan E. Shamseldin,
Saeed Al Tala,
Jamileh Rezazadeh Varaghchi,
Maryam Najafi,
Selina Deschner,
Dieter Gläser,
Wolfgang Hüttel,
Michael C. Kruer,
Erik-Jan Kamsteeg,
Yoshihisa Takiyama,
Stephan Züchner,
Jonathan Baets,
Matthis Synofzik,
Rebecca Schüle,
Rita Horváth,
Henry Houlden,
Luca Bartesaghi,
HweiJen Lee,
Konstantinos Ampatzis,
Tyler Mark Pierson,
Jan Senderek
Publication year - 2021
Publication title -
brain
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.142
H-Index - 336
eISSN - 1460-2156
pISSN - 0006-8950
DOI - 10.1093/brain/awab193
Subject(s) - hereditary spastic paraplegia , spastic , paraplegia , medicine , psychology , genetics , dermatology , physical medicine and rehabilitation , psychiatry , biology , spinal cord , phenotype , cerebral palsy , gene
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom