A spotter’s guide to SNPtic exons: The common splice variants underlying some SNP–phenotype correlations-Reference-Cited by-同舟云学术

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A spotter’s guide to SNPtic exons: The common splice variants underlying some SNP–phenotype correlations

Published:2021-10-28 Issue:1 Volume:10 Page:
ISSN:2324-9269
Container-title:Molecular Genetics & Genomic Medicine
language:en
Short-container-title:Molec Gen & Gen Med

Author:

Keegan Niall Patrick¹²³^ORCID,Fletcher Sue¹²⁴^ORCID

Affiliation:

1. Murdoch University Murdoch Western Australia Australia

2. Centre for Molecular Medicine and Innovative Therapeutics Perth Western Australia Australia

3. Perron Institute Perth Western Australia Australia

4. University of Western Australia Perth Western Australia Australia

Publisher

Wiley

Subject

Genetics (clinical),Genetics,Molecular Biology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.1840

Reference83 articles.

1. Possible role of preproghrelin gene polymorphisms in susceptibility to bulimia nervosa

2. Targeting Poison Exons to Treat Developmental and Epileptic Encephalopathy

3. Whole Genome Sequencing Improves Outcomes of Genetic Testing in Patients With Hypertrophic Cardiomyopathy

4. GWAS Central: a comprehensive resource for the discovery and comparison of genotype and phenotype data from genome‐wide association studies;Beck T.;Nucleic Acids Research,2020

Cited by 1 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. Genetic risk variants for multiple sclerosis are linked to differences in alternative pre-mRNA splicing;Frontiers in Immunology;2022-10-28

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