A mutation in the saposin A domain of the sphingolipid activator protein (prosaposin) gene results in a late-onset, chronic form of globoid cell leukodystrophy in the mouse-Reference-Cited by-同舟云学术

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A mutation in the saposin A domain of the sphingolipid activator protein (prosaposin) gene results in a late-onset, chronic form of globoid cell leukodystrophy in the mouse

Published:2001-05-01 Issue:11 Volume:10 Page:1191-1199
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:
Short-container-title:

Author:

Matsuda J.

Publisher

Oxford University Press (OUP)

Subject

Genetics(clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/10/11/1191/9813461/101191.pdf

Cited by 142 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

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2. Lysosomal storage diseases. Sphingolipidoses – leukodystrophy;Pediatrician (St. Petersburg);2024-05-07

3. Prosaposin is cleaved into saposins by multiple cathepsins in a progranulin-regulated fashion;2024-02-16

4. Krabbe Disease–To Add or Not to Newborn Screening?;OBM Genetics;2024-01-12

5. Glycosphingolipids and central nervous system–related diseases;Glycosphingolipids in the Central Nervous System;2024

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