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Seven mutations in the human insulin gene linked to permanent neonatal/infancy-onset diabetes mellitus
Permanent neonatal diabetes mellitus (PNDM) is a rare disorder usually presenting within 6 months of birth. Although several genes have been linked to this disorder, in almost half the cases documented in Italy, the genetic cause remains unknown. Because the Akita mouse bearing a mutation in the Ins...
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| Autori principali: | , , , , , , , , , , , , , , , , , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
American Society for Clinical Investigation
2008
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2350430/ https://ncbi.nlm.nih.gov/pubmed/18451997 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/JCI33777 |
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