Concepedia

Publication | Open Access

Biallelic Mutations in TMEM126B Cause Severe Complex I Deficiency with a Variable Clinical Phenotype

DOIFull Paper Access

69

Citations

28

References

2016

Year

Charlotte L. Alston, Alison G. Compton, Luke E. Formosa, Valentina Strecker, Monika Oláhová, Tobias B. Haack, Joél Smet, Katrien Stouffs, Peter Diakumis, Elżbieta Ciara,
The American Journal of Human Genetics

References

YearCitations

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