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Missense NAA20 variants impairing the NatB protein N-terminal acetyltransferase cause autosomal recessive developmental delay, intellectual disability, and microcephaly.
Genet Med. 2021 Nov;23(11):2213-2218. doi: 10.1038/s41436-021-01264-0. Epub 2021 Jul 6.
Genet Med. 2021.
PMID: 34230638
Free PMC article.
Further delineation of SMG9-related heart and brain malformation syndrome.
Altuwaijri N, Abdelbaky M, Alhashem A, Alrakaf M, Hashem M, Alzahrani F, Alkuraya FS.
Altuwaijri N, et al.
Am J Med Genet A. 2021 May;185(5):1624-1630. doi: 10.1002/ajmg.a.62139. Epub 2021 Feb 20.
Am J Med Genet A. 2021.
PMID: 33609422
No abstract available.
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A null founder variant in NPNT, encoding nephronectin, causes autosomal recessive renal agenesis.
Al-Hamed MH, Altuwaijri N, Alsahan N, Ali W, Abdulwahab F, Alzahrani F, Majrashi N, Alkuraya FS.
Al-Hamed MH, et al.
Clin Genet. 2022 Jul;102(1):61-65. doi: 10.1111/cge.14128. Epub 2022 Mar 22.
Clin Genet. 2022.
PMID: 35246978
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