Clinical features of two Japanese siblings of neuronal ceroid lipofuscinosis type 1 (CLN1) complicated with TypeⅡ diabetes mellitus-Reference-Cited by-同舟云学术

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Clinical features of two Japanese siblings of neuronal ceroid lipofuscinosis type 1 (CLN1) complicated with TypeⅡ diabetes mellitus

Published:2023-12 Issue: Volume:37 Page:101019
ISSN:2214-4269
Container-title:Molecular Genetics and Metabolism Reports
language:en
Short-container-title:Molecular Genetics and Metabolism Reports

Author:

Eto Kaoru,Itagaki Rina,Takamura Ayumi,Eto Yoshikatsu,Nagata Satoru

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology

Reference19 articles.

1. Genetic basis and phenotypic correlations of the neuronal ceroid lipofusinoses;Warrier;Biochim. Biophys. Acta,1832

2. Neuronal ceroid lipofuscinoses in childhood;Santavuori;Neurol. Sci.,2000

3. Molecular genetics of the NCLs -status and perspectives;Siintola;Biochim. Biophys. Acta,2006

4. NCL diseases - clinical perspectives;Schulz;Biochim. Biophys. Acta,1832

5. Correlation among genotype, phenotype, and histology in neuronal ceroid lipofuscinoses; an individual patient data meta-analysis;Aungaroon;Pediatr. Neurol.,2016

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