Publication
| Sege-Peterson K, Chambers J, Page T, Jones OW, Nyhan WL, Characterization of mutations in phenotypic variants of hypoxanthine phosphoribosyltransferase deficiency. Hum Mol Genet1(6):427-32 1992 |
| PubMed ID: 1301916 |
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| Records Return:
(3)
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| Catalog ID | Gender | Age at Sampling | Description | Collection_Type_id |
| GM20392 | Male | 23 YR | LESCH-NYHAN SYNDROME; LNS | GM |
| GM20396 | Male | 1 MO | LESCH-NYHAN SYNDROME; LNS | GM |
| GM20397 | Male | | LESCH-NYHAN SYNDROME; LNS | GM |
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