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Loss of the sphingolipid desaturase DEGS1 causes hypomyelin..:

Pant, Devesh C ; Dorboz, Imen ; Schlüter, Agatha...
Reproducció del document publicat a: https://doi.org/10.1172/JCI123959. , 2019

Link: http://hdl.handle.net/2445/171613

RT Journal
T1 <Title>Loss of the sphingolipid desaturase DEGS1 causes hypomyelinating leukodystrophy</Title>

UL https://suche.suub.uni-bremen.de/peid=base-ftubarcepubl:oai:diposit.ub.edu:2445_171613&Exemplar=1&LAN=DE
				
A1 Pant, Devesh C
A1 Dorboz, Imen
A1 Schlüter, Agatha
A1 Fourcade, Stéphane
A1 Launay, Nathalie
A1 Joya, Javier
A1 Aguilera Albesa, Sergio
A1 Yoldi, Maria Eugenia
A1 Casasnovas Pons, Carlos
A1 Willis, Mary J
A1 Ruiz, Montserrat
A1 Ville, Dorothée
A1 Lesca, Gaetan
A1 Siquier Pernet, Karine
A1 Desguerre, Isabelle
A1 Yan, Huifang
A1 Wang, Jingmin
A1 Burmeister, Margit
A1 Brady, Lauren
A1 Tarnopolsky, Mark
A1 Cornet, Carles
A1 Rubbini, Davide
A1 Terriente, Javier
A1 James, Kiely N
A1 Musaev, Damir
A1 Zaki, Maha S
A1 Patterson, Marc C
A1 Lanpher, Brendan C
A1 Klee, Eric W
A1 Pinto e Vairo, Filippo
A1 Wohler, Elizabeth
A1 Sobreira, Nara Lygia de M
A1 Cohen, Julie S
A1 Maroofian, Reza
A1 Galehdari, Hamid
A1 Mazaheri, Neda
A1 Shariati, Gholamrez
A1 Colleaux, Laurence
A1 Rodriguez, Diana
A1 Gleeson, Joseph G
A1 Pujades, Cristina
A1 Fatemi, Ali
A1 Boespflug‐Tanguy, Odile
A1 Pujol Onofre, Aurora
PB American Society for Clinical Investigation
YR 2019
K1 Malalties hereditàries
K1 Neurociències
K1 Genetic disorders
K1 Neurosciences
JF Reproducció del document publicat a: https://doi.org/10.1172/JCI123959
LK http://hdl.handle.net/2445/171613
DO http://hdl.handle.net/2445/171613
SF ELIB - SuUB Bremen

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