लोड हो रहा है...
Alms1-disrupted mice recapitulate human Alström syndrome
Mutations in the human ALMS1 gene cause Alström syndrome (AS), a progressive disease characterized by neurosensory deficits and by metabolic defects including childhood obesity, hyperinsulinemia and Type 2 diabetes. Other features that are more variable in expressivity include dilated cardiomyopathy...
में बचाया:
| मुख्य लेखकों: | , , , , , , , , , , |
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| स्वरूप: | Artigo |
| भाषा: | Inglês |
| प्रकाशित: |
2005
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| विषय: | |
| ऑनलाइन पहुंच: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2862911/ https://ncbi.nlm.nih.gov/pubmed/16000322 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddi235 |
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