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1 Ergebnisse
1
Heterozygous PNPT1 variants cause spinocerebellar ataxia ty..:
Barbier, Mathieu
;
Bahlo, Melanie
;
Pennisi, Alessandra
...
info:eu-repo/semantics/altIdentifier/pmid/35411967. , 2022
Link:
http://hdl.handle.net/2318/1854166
RT Journal T1
Heterozygous PNPT1 variants cause spinocerebellar ataxia type 25
UL https://suche.suub.uni-bremen.de/peid=base-ftunivtorino:oai:iris.unito.it:2318_1854166&Exemplar=1&LAN=DE A1 Barbier, Mathieu A1 Bahlo, Melanie A1 Pennisi, Alessandra A1 Jacoupy, Maxime A1 Tankard, Rick M A1 Ewenczyk, Claire A1 Davies, Kayli C A1 Lino-Coulon, Patricia A1 Colace, Claire A1 Rafehi, Haloom A1 Auger, Nicolas A1 Ansell, Brendan R E A1 van der Stelt, Ivo A1 Howell, Katherine B A1 Coutelier, Marie A1 Amor, David J A1 Mundwiller, Emeline A1 Guillot-Noël, Lena A1 Storey, Elsdon A1 Gardner, R J McKinlay A1 Wallis, Mathew J A1 Brusco, Alfredo A1 Corti, Olga A1 Rötig, Agnès A1 Leventer, Richard J A1 Brice, Alexis A1 Delatycki, Martin B A1 Stevanin, Giovanni A1 Lockhart, Paul J A1 Durr, Alexandra YR 2022 K1 spinocerebellar ataxia K1 PNPT1 K1 SCA25 K1 cerebellum JF info:eu-repo/semantics/altIdentifier/pmid/35411967 LK http://hdl.handle.net/2318/1854166 DO http://hdl.handle.net/2318/1854166 SF ELIB - SuUB Bremen
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