BAYAT, Allan; 						JUUL, Annika Wollenberg.
 Mild Lesch-Nyhan disease in a boy with a null-mutation in HPRT1: an exception to the known genotype-phenotype correlation: three-year follow up..
<strong>Medical Research Archives</strong>, [S.l.], v. 4, n. 6, oct. 2016.
ISSN 2375-1924.
Available at: &lt;<a href="https://esmed.org/MRA/mra/article/view/667" target="_new">https://esmed.org/MRA/mra/article/view/667</a>&gt;. Date accessed: 18 nov. 2024.