Cln3 ‐mutations underlying juvenile NCL cause...

Journal of Inherited Metabolic Disease 2019 / 04

Cln3 ‐mutations underlying juvenile NCL cause significantly reduced levels of Ppt1‐protein and Ppt1‐enzyme activity in the lysosome

Appu, Abhilash P., Bagh, Maria B., Sadhukhan, Tamal, Mondal, Avisek, Casey, Sydney, Mukherjee, Anil B.
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Language:
english
Journal:
Journal of Inherited Metabolic Disease
DOI:
10.1002/jimd.12106
Date:
April, 2019
File:
PDF, 1.73 MB
english, 2019
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