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Making sense of missense variants in TTN-related congenital..:

Rees, Martin ; Nikoopour, Roksana ; Fukuzawa, Atsushi...
info:eu-repo/semantics/altIdentifier/doi/10.1007/s00401-020-02257-0. , 2021

Link: https://hal.science/hal-03156853

RT Journal
T1 <Title>Making sense of missense variants in TTN-related congenital myopathies</Title>

UL https://suche.suub.uni-bremen.de/peid=base-ftsorbonneuniv:oai:HAL:hal-03156853v2&Exemplar=1&LAN=DE
				
A1 Rees, Martin
A1 Nikoopour, Roksana
A1 Fukuzawa, Atsushi
A1 Kho, Ay Lin
A1 Fernandez-Garcia, Miguel, A
A1 Wraige, Elizabeth
A1 Bodi, Istvan
A1 Deshpande, Charu
A1 Özdemir, Özkan
A1 Daimagüler, Hülya-Sevcan
A1 Pfuhl, Mark
A1 Holt, Mark
A1 Brandmeier, Birgit
A1 Grover, Sarah
A1 Fluss, Joël
A1 Longman, Cheryl
A1 Farrugia, Maria Elena
A1 Matthews, Emma
A1 Hanna, Michael
A1 Muntoni, Francesco
A1 Sarkozy, Anna
A1 Phadke, Rahul
A1 Quinlivan, Ros
A1 Oates, Emily, C
A1 Schröder, Rolf
A1 Thiel, Christian
A1 Reimann, Jens
A1 Voermans, Nicol
A1 Erasmus, Corrie
A1 Kamsteeg, Erik-Jan
A1 Konersman, Chaminda
A1 Grosmann, Carla
A1 Mckee, Shane
A1 Tirupathi, Sandya
A1 Moore, Steven, A
A1 Wilichowski, Ekkehard
A1 Hobbiebrunken, Elke
A1 Dekomien, Gabriele
A1 Richard, Isabelle
A1 van den Bergh, Peter
A1 Domínguez-González, Cristina
A1 Cirak, Sebahattin
A1 Ferreiro, Ana
A1 Jungbluth, Heinz
A1 Gautel, Mathias
PB HAL CCSD; Springer Verlag
YR 2021
K1 [SDV.GEN.GH]Life Sciences [q-bio]/Genetics/Human genetics
K1 [SDV.MHEP]Life Sciences [q-bio]/Human health and pathology
K1 [SDV.BBM.BM]Life Sciences [q-bio]/Biochemistry
K1 Molecular Biology/Molecular biology
JF info:eu-repo/semantics/altIdentifier/doi/10.1007/s00401-020-02257-0
LK http://dx.doi.org/https://hal.science/hal-03156853
DO https://hal.science/hal-03156853
SF ELIB - SuUB Bremen

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