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Inosinate Pyrophosphorylase Activity in Immature Blood Cells in X-linked Congenital Hyperuricosuria

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Journal Biochem Genet
Specialty Molecular Biology
Date 1969 Aug 1
PMID 5365507
Citations 1
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Citing Articles

[Lesch-Nyhan syndrome. Heterozygote detection by biochemical selection of the mutant cells and autoradiography].

Hagemeijer A, DODINVAL P, Andrien J Humangenetik. 1972; 15(2):126-35.

PMID: 5049065 DOI: 10.1007/BF00295739.

References
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DANCIS J, BERMAN P, Jansen V, BALIS M . Absence of mosaicism in the lymphocyte in X-linked congenital hyperuricosuria. Life Sci. 1968; 7(12):587-91. DOI: 10.1016/0024-3205(68)90079-9. View

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BALIS M, KRAKOFF I, BERMAN P, DANCIS J . Urinary metabolites in congenital hyperuricosuria. Science. 1967; 156(3778):1122-3. DOI: 10.1126/science.156.3778.1122. View

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