Different mutations in Polish patients with HPRT deficiency - The Lesch-Nyhan and Kelley-Seegmiller syndromes
Autor: | Popowska, E., Anna Sulek, Kubalska, J., Pronicka, E., Jezewska, M., Trembacz, H., Goryluk-Kozakiewicz, B., Krajewska-Walasek, M. |
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Zdroj: | Scopus-Elsevier |
Databáze: | OpenAIRE |
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