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1 Ergebnisse
1
Congenital Titinopathy: Comprehensive characterization and ..:
Oates, Emily
;
Jones, Kristi, J
;
Donkervoort, Sandra
...
info:eu-repo/semantics/altIdentifier/doi/10.1002/ana.25241. , 2018
Link:
https://hal.science/hal-02333009
RT Journal T1
Congenital Titinopathy: Comprehensive characterization and pathogenic insights
UL https://suche.suub.uni-bremen.de/peid=base-ftecolephe:oai:HAL:hal-02333009v1&Exemplar=1&LAN=DE A1 Oates, Emily A1 Jones, Kristi, J A1 Donkervoort, Sandra A1 Charlton, Amanda A1 Brammah, Susan A1 Smith, John A1 Ware, James A1 Yau, Kyle A1 Swanson, Lindsay A1 Whiffin, Nicola A1 Peduto, Anthony A1 Bournazos, Adam A1 Waddell, Leigh, B A1 Farrar, Michelle A1 Sampaio, Hugo A1 Teoh, Hooi Ling A1 Lamont, Phillipa A1 Mowat, David A1 Fitzsimons, Robin A1 Corbett, Alastair A1 Ryan, Monique A1 O'Grady, Gina A1 Sandaradura, Sarah A1 Ghaoui, Roula A1 Joshi, Himanshu A1 Marshall, Jamie A1 Nolan, Melinda A1 Kaur, Simranpreet A1 Punetha, Jaya A1 Töpf, Ana A1 Harris, Elizabeth A1 Bakshi, Madhura A1 Genetti, Casie A1 Marttila, Minttu A1 Werlauff, Ulla A1 Streichenberger, Nathalie A1 Pestronk, Alan A1 Mazanti, Ingrid A1 Pinner, Jason A1 Vuillerot, Carole A1 Grosmann, Carla A1 Camacho, Ana A1 Mohassel, Payam A1 Leach, Meganne A1 Foley, a Reghan A1 Bharucha-Goebel, Diana, X A1 Collins, James A1 Connolly, Anne A1 Gilbreath, Heather A1 Iannaccone, Susan A1 Castro, Diana A1 Cummings, Beryl A1 Webster, Richard A1 Lazaro, Leila A1 Vissing, John A1 Coppens, Sandra A1 Deconinck, Nicolas A1 Luk, Ho-Ming A1 Thomas, Neil A1 Foulds, Nicola A1 Illingworth, Marjorie A1 Ellard, Sian A1 Mclean, Catriona A1 Phadke, Rahul A1 Ravenscroft, Gianina A1 Witting, Nanna A1 Hackman, Peter A1 Richard, Isabelle A1 Cooper, Sandra, T A1 Kamsteeg, Erik-Jan A1 Hoffman, Eric A1 Bushby, Kate A1 Straub, Volker A1 Udd, Bjarne A1 Ferreiro, Ana A1 North, Kathryn, N A1 Clarke, Nigel, F A1 Lek, Monkol A1 Beggs, Alan, H A1 Bönnemann, Carsten A1 Macarthur, Daniel A1 Granzier, Henk A1 Davis, Mark A1 Laing, Nigel, G A1 Foley, A. Reghan A1 Bharucha‐goebel, Diana A1 Luk, Ho‐ming A1 Kamsteeg, Erik‐jan PB HAL CCSD; Wiley YR 2018 K1 MESH: Cardiomyopathy K1 Dilated K1 MESH: Connectin K1 MESH: Female K1 MESH: Humans K1 MESH: Male K1 MESH: Muscle Proteins K1 MESH: Muscle K1 Skeletal K1 MESH: Mutation K1 MESH: Phenotype K1 MESH: Protein Isoforms K1 [SDV.BBM.BM]Life Sciences [q-bio]/Biochemistry K1 Molecular Biology/Molecular biology K1 [SDV.BIO]Life Sciences [q-bio]/Biotechnology K1 [SDV.GEN.GH]Life Sciences [q-bio]/Genetics/Human genetics JF info:eu-repo/semantics/altIdentifier/doi/10.1002/ana.25241 LK http://dx.doi.org/https://hal.science/hal-02333009 DO https://hal.science/hal-02333009 SF ELIB - SuUB Bremen
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