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Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1975 1
1977 1
1984 3
1986 2
1987 1
1995 1
1997 1
1998 1
2003 1
2004 1
2007 1
2009 1
2011 1
2012 2
2017 1
2020 1
2022 1
2023 0

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PubMed for id: 811441

21 results

Results by year

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Page 1
Rare and potential pathogenic mutations of LMNA and LAMA4 associated with familial arrhythmogenic right ventricular cardiomyopathy/dysplasia with right ventricular heart failure, cerebral thromboembolism and hereditary electrocardiogram abnormality.
Chen J, Ma Y, Li H, Lin Z, Yang Z, Zhang Q, Wang F, Lin Y, Ye Z, Lin Y. Chen J, et al. Orphanet J Rare Dis. 2022 May 7;17(1):183. doi: 10.1186/s13023-022-02348-z. Orphanet J Rare Dis. 2022. PMID: 35526016 Free PMC article.
Human KCNQ1 S140G mutation is associated with atrioventricular blocks.
Yang Y, Liu Y, Dong X, Kuang Y, Lin J, Su X, Peng L, Jin Q, He Y, Liu B, Pan Z, Li L, Zhu Q, Lin X, Zhou Q, Pan Q, Eurlings PM, Fei J, Wang Z, Chen YH. Yang Y, et al. Heart Rhythm. 2007 May;4(5):611-8. doi: 10.1016/j.hrthm.2007.01.029. Epub 2007 Feb 1. Heart Rhythm. 2007. PMID: 17467630
21 results