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Biallelic variants in HPDL cause pure and complicated hered..:
Wiessner, Manuela
;
Maroofian, Reza
;
Ni, Meng-Yuan
...
qt3zq3c14v. , 2021
Link:
https://escholarship.org/uc/item/3zq3c14v
RT Journal T1
Biallelic variants in HPDL cause pure and complicated hereditary spastic paraplegia
UL https://suche.suub.uni-bremen.de/peid=base-ftcdlib:oai:escholarship.org:ark:_13030_qt3zq3c14v&Exemplar=1&LAN=DE A1 Wiessner, Manuela A1 Maroofian, Reza A1 Ni, Meng-Yuan A1 Pedroni, Andrea A1 Müller, Juliane S A1 Stucka, Rolf A1 Beetz, Christian A1 Efthymiou, Stephanie A1 Santorelli, Filippo M A1 Alfares, Ahmed A A1 Zhu, Changlian A1 Uhrova Meszarosova, Anna A1 Alehabib, Elham A1 Bakhtiari, Somayeh A1 Janecke, Andreas R A1 Otero, Maria Gabriela A1 Chen, Jin Yun Helen A1 Peterson, James T A1 Strom, Tim M A1 De Jonghe, Peter A1 Deconinck, Tine A1 De Ridder, Willem A1 De Winter, Jonathan A1 Pasquariello, Rossella A1 Ricca, Ivana A1 Alfadhel, Majid A1 van de Warrenburg, Bart P A1 Portier, Ruben A1 Bergmann, Carsten A1 Ghasemi Firouzabadi, Saghar A1 Jin, Sheng Chih A1 Bilguvar, Kaya A1 Hamed, Sherifa A1 Abdelhameed, Mohammed A1 Haridy, Nourelhoda A A1 Maqbool, Shazia A1 Rahman, Fatima A1 Anwar, Najwa A1 Carmichael, Jenny A1 Pagnamenta, Alistair A1 Wood, Nick W A1 Tran Mau-Them, Frederic A1 Haack, Tobias A1 Di Rocco, Maja A1 Ceccherini, Isabella A1 Iacomino, Michele A1 Zara, Federico A1 Salpietro, Vincenzo A1 Scala, Marcello A1 Rusmini, Marta A1 Xu, Yiran A1 Wang, Yinghong A1 Suzuki, Yasuhiro A1 Koh, Kishin A1 Nan, Haitian A1 Ishiura, Hiroyuki A1 Tsuji, Shoji A1 Lambert, Laëtitia A1 Schmitt, Emmanuelle A1 Lacaze, Elodie A1 Küpper, Hanna A1 Dredge, David A1 Skraban, Cara A1 Goldstein, Amy A1 Willis, Mary JH A1 Grand, Katheryn A1 Graham, John M A1 Lewis, Richard A A1 Millan, Francisca A1 Duman, Özgür A1 Dündar, Nihal A1 Uyanik, Gökhan A1 Schöls, Ludger A1 Nürnberg, Peter A1 Nürnberg, Gudrun A1 Catala Bordes, Andrea A1 Seeman, Pavel A1 Kuchar, Martin A1 Darvish, Hossein A1 Rebelo, Adriana A1 Bouçanova, Filipa A1 Medard, Jean-Jacques A1 Chrast, Roman A1 Auer-Grumbach, Michaela A1 Alkuraya, Fowzan S A1 Shamseldin, Hanan A1 Al Tala, Saeed A1 Rezazadeh Varaghchi, Jamileh A1 Najafi, Maryam A1 Deschner, Selina A1 Gläser, Dieter A1 Hüttel, Wolfgang A1 Kruer, Michael C A1 Kamsteeg, Erik-Jan A1 Takiyama, Yoshihisa A1 Züchner, Stephan A1 Baets, Jonathan A1 Synofzik, Matthis A1 Schüle, Rebecca A1 Horvath, Rita PB eScholarship, University of California YR 2021 K1 Neurosciences K1 Neurodegenerative K1 Genetics K1 Clinical Research K1 Aetiology K1 2.1 Biological and endogenous factors K1 Neurological K1 Animals K1 Female K1 Humans K1 Male K1 Mice K1 Mutation K1 Oxygenases K1 Pedigree K1 Rats K1 Spastic Paraplegia K1 Hereditary K1 Zebrafish K1 hereditary spastic paraplegia K1 HSP K1 autosomal recessive K1 mitochondrial disorder K1 HPDL K1 Genomics England Research Consortium K1 PREPARE network K1 Medical and Health Sciences K1 Psychology and Cognitive Sciences K1 Neurology & Neurosurgery JF qt3zq3c14v LK http://dx.doi.org/https://escholarship.org/uc/item/3zq3c14v DO https://escholarship.org/uc/item/3zq3c14v SF ELIB - SuUB Bremen
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