Biallelic Mutations in TMEM126B Cause Severe Complex I Deficiency with a Variable Clinical Phenotype (Q37218530)
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scientific article published on 29 June 2016
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Biallelic Mutations in TMEM126B Cause Severe Complex I Deficiency with a Variable Clinical Phenotype |
scientific article published on 29 June 2016 |
Statements
1 reference
Biallelic Mutations in TMEM126B Cause Severe Complex I Deficiency with a Variable Clinical Phenotype (English)
1 reference
Robert W Taylor
Valentina Strecker
Monika Oláhová
Joél Smet
Nadine Romain
John W Yarham
Langping He
Boel De Paepe
Arnaud V Vanlander
Sara Seneca
René G Feichtinger
Ronald G Haller
Johan L K Van Hove
Rudy Van Coster
29 June 2016
1 reference