Long-Term Disease Course of Pontocerebellar Hypoplasia Type 10-Reference-Cited by-同舟云学术

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Long-Term Disease Course of Pontocerebellar Hypoplasia Type 10

Published:2024-09 Issue: Volume:158 Page:1-10
ISSN:0887-8994
Container-title:Pediatric Neurology
language:en
Short-container-title:Pediatric Neurology

Author:

Guler Serhat^ORCID,Aslanger Ayca Dilruba^ORCID,Uygur Sahin Turkan^ORCID,Alkan Alpay^ORCID,Yalcinkaya Cengiz^ORCID,Saltik Sema^ORCID,Yesil Gözde^ORCID

Publisher

Elsevier BV

Reference15 articles.

1. Human CLP1 mutations alter tRNA biogenesis, affecting both peripheral and central nervous system function;Karaca;Cell,2014

2. CLP1 founder mutation links tRNA splicing and maturation to cerebellar development and neurodegeneration;Schaffer;Cell,2014

3. The human RNA kinase hClp1 is active on 3' transfer RNA exons and short interfering RNAs;Weitzer;Nature,2007

4. CLP1 links tRNA metabolism to progressive motor-neuron loss;Hanada;Nature,2013

5. The Clp1 R140H mutation alters tRNA metabolism and mRNA 3' processing in mouse models of pontocerebellar hypoplasia;Monaghan;Proc Natl Acad Sci U S A,2021

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