Uniparental disomy of chromosome 1 causing concurrent Charcot-Marie-Tooth and Gaucher disease Type 3.
| Autor: | Benko WS, Hruska KS, Nagan N, Goker-Alpan O, Hart PS, Schiffmann R, Sidransky E, Benko, W S, Hruska, K S, Nagan, N, Goker-Alpan, O, Hart, P S, Schiffmann, R, Sidransky, E |
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| Zdroj: | Neurology; 3/18/2008, Vol. 70 Issue 12, p976-978, 3p |
| Databáze: | Supplemental Index |
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