Natural History of Neuronal Ceroid Lipofuscinosis Type 6, Late Infantile Disease-Reference-Cited by-同舟云学术

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Natural History of Neuronal Ceroid Lipofuscinosis Type 6, Late Infantile Disease

Published:2024-05 Issue: Volume:154 Page:51-57
ISSN:0887-8994
Container-title:Pediatric Neurology
language:en
Short-container-title:Pediatric Neurology

Author:

O'Neal Matthew,Noher de Halac Ines^ORCID,Aylward Shawn C.^ORCID,Yildiz Vedat,Zapanta Bianca,Abreu Nicolas^ORCID,de los Reyes Emily^ORCID

Publisher

Elsevier BV

Reference16 articles.

1. Neurodegenerative diseases of infancy and childhood;Dyken;J Child Neurol,1983

2. The neuronal ceroid lipofuscinosis;Dyken;J Child Neurol,1989

3. Moving towards a new era of genomics in the neuronal ceroid lipofuscinosis;Butz;Biochim Biophys Acta Mol Basis Dis,2020

4. Loci for classical and a variant late infantile neuronal ceroid lipofuscinosis map to chromosomes 1115 and 15q21-23;Sharp;Hum Mol Genet,1997

5. CLN6, which is associated with a lysosomal storage disease, is an endoplasmic reticulum protein;Mole;Exp Cell Res,2004

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