Infantile mitochondrial encephalomyopathy with unusual phenotype caused by a novel BCS1L mutation in an isolated complex III-deficient patient. (Q54497626)
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scientific article
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Infantile mitochondrial encephalomyopathy with unusual phenotype caused by a novel BCS1L mutation in an isolated complex III-deficient patient. |
scientific article |
Statements
Infantile mitochondrial encephalomyopathy with unusual phenotype caused by a novel BCS1L mutation in an isolated complex III-deficient patient. (English)
Alberto Blázquez
Mari Carmen Gil-Borlado
María Morán
Alfonso Verdú
María Rosario Cazorla-Calleja
Miguel A Martín
Joaquín Arenas
Cristina Ugalde
21 January 2009
19
2
143-146