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A Novel Missense Mutation in TNNI3K Causes Recessively Inherited Cardiac Conduction Disease in a Consanguineous Pakistani Family.
Genes (Basel). 2021 Aug 21;12(8):1282. doi: 10.3390/genes12081282.
Genes (Basel). 2021.
PMID: 34440456
Free PMC article.
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: korejo aa.
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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Homozygous frameshift variant in desmoglein 2 gene causes biventricular arrhythmogenic right ventricular cardiomyopathy.
Noor Ul Ayan H, Ali PS, Korejo AA, Thiele H, Nürnberg P, Tariq M, Jamal SZ, Erdmann J, Ahmad I.
Noor Ul Ayan H, et al. Among authors: korejo aa.
Clin Genet. 2023 Aug;104(2):266-268. doi: 10.1111/cge.14321. Epub 2023 Mar 12.
Clin Genet. 2023.
PMID: 36843528
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Molecular surveillance of HCV mono-infection and HCV-HBV co-infection in symptomatic population at Hyderabad, Pakistan.
Patoli BB, Patoli AA, Balani NK, Korejo AA.
Patoli BB, et al. Among authors: korejo aa.
Afr Health Sci. 2018 Sep;18(3):531-538. doi: 10.4314/ahs.v18i3.9.
Afr Health Sci. 2018.
PMID: 30602984
Free PMC article.
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