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1 Ergebnisse
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Biallelic Mutations in TMEM126B Cause Severe Complex I Defi..:
Alston, Charlotte L.
;
Compton, Alison G.
;
Formosa, Luke E.
...
The American Journal of Human Genetics. 99 (2016) 1 - p. 217-227 , 2016
Link:
https://doi.org/10.1016/j.ajhg.2016.05.021
RT Journal T1
Biallelic Mutations in TMEM126B Cause Severe Complex I Deficiency with a Variable Clinical Phenotype
UL https://suche.suub.uni-bremen.de/peid=cr-10.1016_j.ajhg.2016.05.021&Exemplar=1&LAN=DE A1 Alston, Charlotte L. A1 Compton, Alison G. A1 Formosa, Luke E. A1 Strecker, Valentina A1 Oláhová, Monika A1 Haack, Tobias B. A1 Smet, Joél A1 Stouffs, Katrien A1 Diakumis, Peter A1 Ciara, Elżbieta A1 Cassiman, David A1 Romain, Nadine A1 Yarham, John W. A1 He, Langping A1 De Paepe, Boel A1 Vanlander, Arnaud V. A1 Seneca, Sara A1 Feichtinger, René G. A1 Płoski, Rafal A1 Rokicki, Dariusz A1 Pronicka, Ewa A1 Haller, Ronald G. A1 Van Hove, Johan L.K. A1 Bahlo, Melanie A1 Mayr, Johannes A. A1 Van Coster, Rudy A1 Prokisch, Holger A1 Wittig, Ilka A1 Ryan, Michael T. A1 Thorburn, David R. PB Elsevier BV YR 2016 SN 0002-9297 JF The American Journal of Human Genetics VO 99 IS 1 SP 217 OP 227 LK http://dx.doi.org/https://doi.org/10.1016/j.ajhg.2016.05.021 DO https://doi.org/10.1016/j.ajhg.2016.05.021 SF ELIB - SuUB Bremen
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