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Impaired Elastogenesis in Hurler Disease : Dermatan Sulfate Accumulation Linked to Deficiency in Elastin-Binding Protein and Elastic Fiber Assembly

Hurler disease resulting from a deficiency in α-l-iduronidase, which causes an accumulation of dermatan sulfate and heparan sulfate glycosaminoglycans, is characterized by connective tissue and skeletal deformations, cardiomyopathy, cardiac valve defects, and progressive coronary artery stenosis. In...

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Detaylı Bibliyografya
Asıl Yazarlar: Hinek, Aleksander, Wilson, Sarah E.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: American Society for Investigative Pathology 2000
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC1876830/
https://ncbi.nlm.nih.gov/pubmed/10702409
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