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[Enzyme defects of purine metabolism].
1979
E Kaiser, and M M Müller
Associated MeSH Terms
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MeSH Term
Description
Entries
D011686
Purine-Pyrimidine Metabolism, Inborn Errors
Dysfunctions in the metabolism of PURINES or PYRIMIDINES resulting from inborn genetic mutations that are inherited or acquired in utero.
Purine Pyrimidine Metabolism, Inborn Errors
D006801
Humans
Members of the species Homo sapiens.
Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
Related Publications
E Kaiser, and M M Müller
Enzyme defects in purine metabolism and immunodeficiencies.
December 1985, Nihon Ketsueki Gakkai zasshi : journal of Japan Haematological Society,
E Kaiser, and M M Müller
[Immune insufficiency in enzyme defects of purine metabolism].
February 1983, Zeitschrift fur die gesamte innere Medizin und ihre Grenzgebiete,
E Kaiser, and M M Müller
Defects of purine metabolism in immunodeficiency diseases.
January 1977, Progress in clinical immunology,
E Kaiser, and M M Müller
Defects in purine metabolism and neurologic disease.
April 1968, Bulletin of the Los Angeles neurological societies,
E Kaiser, and M M Müller
[Enzyme defects of fat metabolism].
September 1971, Wiener klinische Wochenschrift,
E Kaiser, and M M Müller
Genetic defects in human purine and pyrimidine metabolism.
January 1982, Annual review of genetics,
E Kaiser, and M M Müller
Intermediary purine metabolism and the metabolic defects of gout.
May 1957, Metabolism: clinical and experimental,
E Kaiser, and M M Müller
[Enzyme defects in lipid metabolism].
October 1970, Wiener klinische Wochenschrift,
E Kaiser, and M M Müller
[Clinical significance of purine analogs and related enzyme metabolism].
December 1989, Nihon rinsho. Japanese journal of clinical medicine,
E Kaiser, and M M Müller
[Hereditary enzyme defects of amino acid metabolism].
January 1962, Ergebnisse der inneren Medizin und Kinderheilkunde,
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