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Different mutations in Polish patients with HPRT deficiency - the Lesch-Nyhan and Kelley-Seegmiller syndromes
Different mutations in Polish patients with HPRT deficiency - the Lesch-Nyhan and Kelley-Seegmiller syndromes
1998
E Popowska
Anna Sulek
Jolanta Kubalska
Ewa Pronicka
M Jezewska
H. Trembacz
Bożenna Goryluk-Kozakiewicz
Małgorzata Krajewska-Walasek
Keywords:
Genetics
Lesch–Nyhan syndrome
Biology
Point mutation
Kelley-Seegmiller Syndrome
HPRT DEFICIENCY
Correction
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