| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 10882994 | Mitochondrion | 2013 | 7 Pages |
Abstract
The prevalence of SCO2 deficiency in Poland is relatively high. A search for SCO2 mutations in patients with histology resembling SMA appears to efficiently improve the detection rate.
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Authors
Ewa Pronicka, Dorota Piekutowska-Abramczuk, Tamara SzymaÅska-DÄbiÅska, Liliana Bielecka, PaweÅ Kowalski, Sylwia Åuczak, Agnieszka KarkuciÅska-WiÄckowska, Marek MigdaÅ, Jolanta Kubalska, Janusz Zimowski, Ewa Jamroz, Jolanta Wierzba,