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Biallelic variants in HPDL cause pure and complicated hered..:

Wiessner, M ; Maroofian, R ; Ni, M-Y...
https://discovery.ucl.ac.uk/id/eprint/10128647/3/Houlden_BRAIN%202020-01588_manuscript_R1_plain%20copy.pdf. , 2021

Link: https://discovery.ucl.ac.uk/id/eprint/10128647/3/Hould..

RT Journal
T1 <Title>Biallelic variants in HPDL cause pure and complicated hereditary spastic paraplegia</Title>

UL https://suche.suub.uni-bremen.de/peid=base-ftucl:oai:eprints.ucl.ac.uk.OAI2:10128647&Exemplar=1&LAN=DE
				
A1 Wiessner, M
A1 Maroofian, R
A1 Ni, M-Y
A1 Pedroni, A
A1 Müller, JS
A1 Stucka, R
A1 Beetz, C
A1 Efthymiou, S
A1 Santorelli, FM
A1 Alfares, AA
A1 Zhu, C
A1 Uhrova Meszarosova, A
A1 Alehabib, E
A1 Bakhtiari, S
A1 Janecke, AR
A1 Otero, MG
A1 Chen, JYH
A1 Peterson, JT
A1 Strom, TM
A1 De Jonghe, P
A1 Deconinck, T
A1 De Ridder, W
A1 De Winter, J
A1 Pasquariello, R
A1 Ricca, I
A1 Alfadhel, M
A1 van de Warrenburg, BP
A1 Portier, R
A1 Bergmann, C
A1 Ghasemi Firouzabadi, S
A1 Jin, SC
A1 Bilguvar, K
A1 Hamed, S
A1 Abdelhameed, M
A1 Haridy, NA
A1 Maqbool, S
A1 Rahman, F
A1 Anwar, N
A1 Carmichael, J
A1 Pagnamenta, A
A1 Wood, NW
A1 Tran Mau-Them, F
A1 Haack, T
A1 Genomics England Research Consortium, PREPARE network
A1 Di Rocco, M
A1 Ceccherini, I
A1 Iacomino, M
A1 Zara, F
A1 Salpietro, V
A1 Scala, M
A1 Rusmini, M
A1 Xu, Y
A1 Wang, Y
A1 Suzuki, Y
A1 Koh, K
A1 Nan, H
A1 Ishiura, H
A1 Tsuji, S
A1 Lambert, L
A1 Schmitt, E
A1 Lacaze, E
A1 Küpper, H
A1 Dredge, D
A1 Skraban, C
A1 Goldstein, A
A1 Willis, MJH
A1 Grand, K
A1 Graham, JM
A1 Lewis, RA
A1 Millan, F
A1 Duman, Ö
A1 Dündar, N
A1 Uyanik, G
A1 Schöls, L
A1 Nürnberg, P
A1 Nürnberg, G
A1 Catala Bordes, A
A1 Seeman, P
A1 Kuchar, M
A1 Darvish, H
A1 Rebelo, A
A1 Bouçanova, F
A1 Medard, J-J
A1 Chrast, R
A1 Auer-Grumbach, M
A1 Alkuraya, FS
A1 Shamseldin, H
A1 Al Tala, S
A1 Rezazadeh Varaghchi, J
A1 Najafi, M
A1 Deschner, S
A1 Gläser, D
A1 Hüttel, W
A1 Kruer, MC
A1 Kamsteeg, E-J
A1 Takiyama, Y
A1 Züchner, S
A1 Baets, J
A1 Synofzik, M
A1 Schüle, R
A1 Horvath, R
A1 Houlden, H
A1 Bartesaghi, L
A1 Lee, H-J
A1 Ampatzis, K
A1 Pierson, TM
A1 Senderek, J
YR 2021
K1 HPDL
K1 HSP
K1 autosomal recessive
K1 hereditary spastic paraplegia
K1 mitochondrial disorder
JF https://discovery.ucl.ac.uk/id/eprint/10128647/3/Houlden_BRAIN%202020-01588_manuscript_R1_plain%20copy.pdf
LK http://dx.doi.org/https://discovery.ucl.ac.uk/id/eprint/10128647/3/Houlden_BRAIN%202020-01588_manuscript_R1_plain%20copy.pdf
DO https://discovery.ucl.ac.uk/id/eprint/10128647/3/Houlden_BRAIN%202020-01588_manuscript_R1_plain%20copy.pdf
SF ELIB - SuUB Bremen

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