Genetics of Menkes Disease
Fibroblast cultures from 12 unrelated patients with classical Menkes disease, an X-linked disorder of copper metabolism, were analyzed for mutations in the MNK gene at the Howard Hughes Medical Institute, University of California, San Francisco.
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| Formato: | Artigo |
| Idioma: | Inglês |
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Pediatric Neurology Briefs Publishers
1994-11-01
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| Series: | Pediatric Neurology Briefs |
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| Acceso en liña: | https://www.pediatricneurologybriefs.com/articles/2805 |
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