Literature DB >> 3974350

[Lesch-Nyhan syndrome: a new variant with hypoxanthine-guanine phosphoriboxyl transferase activity higher than the classical disease and detection of the heterozygote trait in the erythrocytes of the carrier].

L Hernández Nieto, W L Nyhan, T Page, G Cubillo Ferreira, M Rodríguez Fernández, T González García, A Cabrera de León, F J Santolaria Fernández.   

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Year:  1985        PMID： 3974350

Source DB:  PubMed          Journal:  Med Clin (Barc)        ISSN： 0025-7753            Impact factor:   1.725


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  1 in total

Review 1.  The recognition of Lesch-Nyhan syndrome as an inborn error of purine metabolism.

Authors:  W L Nyhan
Journal:  J Inherit Metab Dis       Date:  1997-06       Impact factor: 4.982
  1 in total

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