A novel mouse model of a patient mucolipidosis II mutation recapitulates disease pathology.
Mucolipidosis II (MLII) is a lysosomal storage disorder caused by loss of N-acetylglucosamine-1-phosphotransferase, which tags lysosomal enzymes with a mannose 6-phosphate marker for transport to the lysosome. In MLII, the loss of this marker leads to deficiency of multiple enzymes and non-enzymatic...
मुख्य लेखकों: | Paton, L, Bitoun, E, Kenyon, J, Priestman, D, Oliver, P, Edwards, B, Platt, F, Davies, K |
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स्वरूप: | Journal article |
भाषा: | English |
प्रकाशित: |
American Society for Biochemistry and Molecular Biology Inc.
2014
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समान संसाधन
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Neurologic abnormalities in mouse models of the lysosomal storage disorders mucolipidosis II and mucolipidosis III γ.
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Correction: Neurologic Abnormalities in Mouse Models of the Lysosomal Storage Disorders Mucolipidosis II and Mucolipidosis III γ
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Correction: Neurologic Abnormalities in Mouse Models of the Lysosomal Storage Disorders Mucolipidosis II and Mucolipidosis III γ.
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