Chromosomal localization of two genes underlying late-infantile neuronal ceroid lipofuscinosis-Reference-Cited by-同舟云学术

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Chromosomal localization of two genes underlying late-infantile neuronal ceroid lipofuscinosis

Published:1998-03-24 Issue:3 Volume:1 Page:217-222
ISSN:1364-6745
Container-title:neurogenetics
language:
Short-container-title:neurogenetics

Author:

Haines J. L.,Boustany Rose-Mary N.,Alroy Joseph,Auger Kristen J.,Shook Kerida S.,Terwedow Henry,Lerner T. J.

Publisher

Springer Science and Business Media LLC

Subject

Cellular and Molecular Neuroscience,Genetics(clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/s100480050032.pdf

Cited by 20 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

1. Neuronal Ceroid Lipofuscinosis Type 6 (CLN6) clinical findings and molecular diagnosis: Costa Rica’s experience;Orphanet Journal of Rare Diseases;2022-01-10

2. Generation of pathogenic TPP1 mutations in human stem cells as a model for neuronal ceroid lipofuscinosis type 2 disease;Stem Cell Research;2021-05

3. Generation of Pathogenic TPP1 Mutations in Human Stem Cells as a Model for CLN2 Disease;2021-01-06

4. Clinical and genetic description of neuronal ceroid lipofuscinosis 6 type in the yakut family;Zhurnal nevrologii i psikhiatrii im. S.S. Korsakova;2021

5. Upregulation of tripeptidyl-peptidase 1 by 3-hydroxy-(2,2)-dimethyl butyrate, a brain endogenous ligand of PPARα: Implications for late-infantile Batten disease therapy;Neurobiology of Disease;2019-07

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