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The Biological Clock and the Molecular Basis of Lysosomal Storage Diseases

The lysosomal storage disorders encompass nearly fifty diseases provoked by lack or deficiency of enzymes essential for the breakdown of complex molecules and hallmarked by accumulation in the lysosomes of metabolic residues. Histochemistry and cytochemistry studies evidenced patterns of circadian v...

詳細記述

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書誌詳細
出版年:JIMD Rep
主要な著者: Mazzoccoli, Gianluigi, Mazza, Tommaso, Vinciguerra, Manlio, Castellana, Stefano, Scarpa, Maurizio
フォーマット: Artigo
言語:Inglês
出版事項: Springer Berlin Heidelberg 2015
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC4361918/
https://ncbi.nlm.nih.gov/pubmed/25583520
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/8904_2014_354
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