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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2021 | 1 |
2022 | 1 |
2023 | 2 |
2024 | 0 |
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Homozygous frameshift variant in desmoglein 2 gene causes biventricular arrhythmogenic right ventricular cardiomyopathy.
Clin Genet. 2023 Aug;104(2):266-268. doi: 10.1111/cge.14321. Epub 2023 Mar 12.
Clin Genet. 2023.
PMID: 36843528
A novel MAP3K20 mutation causing centronuclear myopathy-6 with fiber-type disproportion in a Pakistani family.
Ahmad I, Khan A, Noor Ul Ayan H, Budde B, Altmüller J, Korejo AA, Nürnberg G, Thiele H, Tariq M, Nürnberg P, Erdmann J.
Ahmad I, et al. Among authors: noor ul ayan h.
J Hum Genet. 2023 Feb;68(2):107-109. doi: 10.1038/s10038-022-01085-2. Epub 2022 Oct 11.
J Hum Genet. 2023.
PMID: 36217027
Free PMC article.
No abstract available.
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A Novel Missense Mutation in TNNI3K Causes Recessively Inherited Cardiac Conduction Disease in a Consanguineous Pakistani Family.
Ramzan S, Tennstedt S, Tariq M, Khan S, Noor Ul Ayan H, Ali A, Munz M, Thiele H, Korejo AA, Mughal AR, Jamal SZ, Nürnberg P, Baig SM, Erdmann J, Ahmad I.
Ramzan S, et al. Among authors: noor ul ayan h.
Genes (Basel). 2021 Aug 21;12(8):1282. doi: 10.3390/genes12081282.
Genes (Basel). 2021.
PMID: 34440456
Free PMC article.
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