LYSOSOMAL STORAGE DISEASE

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GHOFRANI MOHAMMAD

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Journal Paper

Paper Information

Journal: Iranian Journal of Child Neurology Year:2012 | Volume:6 | Issue:4 (SUPPL 1) Page(s): 1-2

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Information Journal Paper

Title

LYSOSOMAL STORAGE DISEASE

Author(s)

GHOFRANI MOHAMMAD | Issue Writer Certificate

Keywords

LYSOSOME

ENZYME

GENE THERAPY

CHILD

Abstract

LYSOSOMEs are cytoplasmic organelles containing hydrolytic ENZYMEs that degrade the macromolecules proteins of cellular catabolism. The causes of lysosomal ENZYME disorder stem from1. Impaired ENZYME synthesis2. Abnormal ENZYME targeting3. Defect of structure of Accessory factor which is needed for ENZYMEs function. Clinical manifestations depend on the organ (s) involved.

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APA: Copy

GHOFRANI, MOHAMMAD. (2012). LYSOSOMAL STORAGE DISEASE. IRANIAN JOURNAL OF CHILD NEUROLOGY (IJCN), 6(4 (SUPPL 1)), 1-2. SID. https://sid.ir/paper/303467/en

Vancouver: Copy

GHOFRANI MOHAMMAD. LYSOSOMAL STORAGE DISEASE. IRANIAN JOURNAL OF CHILD NEUROLOGY (IJCN)[Internet]. 2012;6(4 (SUPPL 1)):1-2. Available from: https://sid.ir/paper/303467/en

IEEE: Copy

MOHAMMAD GHOFRANI, “LYSOSOMAL STORAGE DISEASE,” IRANIAN JOURNAL OF CHILD NEUROLOGY (IJCN), vol. 6, no. 4 (SUPPL 1), pp. 1–2, 2012, [Online]. Available: https://sid.ir/paper/303467/en

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