Mutations in the inosine monophosphate dehydrogenase 1 gene (IMPDH1) cause the RP10 form of autosomal dominant retinitis pigmentosa-Reference-Cited by-同舟云学术

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Mutations in the inosine monophosphate dehydrogenase 1 gene (IMPDH1) cause the RP10 form of autosomal dominant retinitis pigmentosa

Published:2002-03-01 Issue:5 Volume:11 Page:559-568
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:
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Author:

Bowne S. J.

Publisher

Oxford University Press (OUP)

Subject

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

Cited by 192 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. Impaired inosine monophosphate dehydrogenase leads to plant-specific ribosomal stress responses in Arabidopsis thaliana;Journal of Plant Research;2024-09-05

2. IMPDH2 filaments protect from neurodegeneration in AMPD2 deficiency;EMBO Reports;2024-07-29

3. Impaired Inosine Monophosphate Dehydrogenase Leads to Plant-Specific Ribosomal Stress Responses in Arabidopsis thaliana;2024-06-05

4. The Impact of Terminal Peptide Extensions of Retinal Inosine 5´Monophosphate Dehydrogenase 1 Isoforms on their DNA-binding Activities;The Protein Journal;2024-05-11

5. Datasets-Based IMPDH1 Revisited: Heterozygous Missense Variants for Dominant Retinitis Pigmentosa While Truncation Variants Are Likely Non-Pathogenic;Current Eye Research;2024-04-11

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