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Alston et al., 2016
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@article{Alston2016, author = {Alston, Charlotte L. and Compton, Alison G. and Formosa, Luke E. and Strecker, Valentina and Oláhová, Monika and Haack, Tobias B. and Smet, Joél and Stouffs, Katrien and Diakumis, Peter and Ciara, Elżbieta and Cassiman, David and Romain, Nadine and Yarham, John W. and He, Langping and De Paepe, Boel and Vanlander, Arnaud V. and Seneca, Sara and Feichtinger, René G. and Płoski, Rafal and Rokicki, Dariusz and Pronicka, Ewa and Haller, Ronald G. and Van Hove, Johan L. K. and Bahlo, Melanie and Mayr, Johannes A. and Van Coster, Rudy and Prokisch, Holger and Wittig, Ilka and Ryan, Michael T. and Thorburn, David R. and Taylor, Robert W.}, doi = {10.1016/j.ajhg.2016.05.021}, month = {jan}, title = {Biallelic Mutations in TMEM126B Cause Severe Complex I Deficiency with a Variable Clinical Phenotype}, url = {http://doi.org/10.1016/j.ajhg.2016.05.021}, year = {2016} }
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Biallelic Mutations in TMEM126B Cause Severe Complex I Deficiency with a Variable Clinical Phenotype
Journal article published in 2016 by
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
and
other authors.
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
,
Ewa Pronicka
,
Ronald G. Haller
,
Johan L. K. Van Hove
,
Melanie Bahlo
,
Johannes A. Mayr
,
Rudy Van Coster
,
Holger Prokisch
,
Ilka Wittig
,
Michael T. Ryan
,
David R. Thorburn
,
Robert W. Taylor
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