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Dive into the research topics of 'Biallelic Mutations in TMEM126B Cause Severe Complex I Deficiency with a Variable Clinical Phenotype'. Together they form a unique fingerprint.- Sort by
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Charlotte L. Alston, Alison G. Compton, Luke E. Formosa, Valentina Strecker, Monika Oláhová, Tobias B. Haack, Joél Smet, Katrien Stouffs, Peter Diakumis, Elżbieta Ciara, David Cassiman, Nadine Romain, John W. Yarham, Langping He, Boel De Paepe, Arnaud V. Vanlander, Sara Seneca, René G. Feichtinger, Rafal Płoski, Dariusz Rokicki
Research output: Contribution to journal › Article › peer-review