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...

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Main Authors: Collin, G.B., Cyr, E., Bronson, R., Marshall, J.D., Gifford, E.J., Hicks, W., Murray, S.A., Zheng, Q.Y., Smith, R.S., Nishina, P.M., Naggert, J.K.
Formáid: Artigo
Teanga:Inglês
Foilsithe: 2005
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Article
Rochtain Ar Líne: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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