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Determinants of Obtaining COVID-19 Vaccination among Health Care Workers with Access to Free COVID-19 Vaccination: A Cross-Sectional Study.
Vaccines (Basel). 2021 Dec 29;10(1):39. doi: 10.3390/vaccines10010039.
Vaccines (Basel). 2021.
PMID: 35062700
Free PMC article.
Review.
Exome Sequencing Identifies a Novel Sorting Nexin 14 Gene Mutation Causing Cerebellar Atrophy and Intellectual Disability.
Al-Hashmi N, Mohammed M, Al-Kathir S, Al-Yarubi N, Scott P.
Al-Hashmi N, et al.
Case Rep Genet. 2018 Oct 24;2018:6737938. doi: 10.1155/2018/6737938. eCollection 2018.
Case Rep Genet. 2018.
PMID: 30473892
Free PMC article.
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Deficiency of acyl-CoA synthetase 5 is associated with a severe and treatable failure to thrive of neonatal onset.
Al-Thihli K, Afting C, Al-Hashmi N, Mohammed M, Sliwinski S, Al Shibli N, Al-Said K, Al-Kasbi G, Al-Kharusi K, Merle U, Füllekrug J, Al-Maawali A.
Al-Thihli K, et al.
Clin Genet. 2021 Mar;99(3):376-383. doi: 10.1111/cge.13883. Epub 2020 Nov 25.
Clin Genet. 2021.
PMID: 33191500
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Biallelic mutations in AP3D1 cause Hermansky-Pudlak syndrome type 10 associated with immunodeficiency and seizure disorder.
Mohammed M, Al-Hashmi N, Al-Rashdi S, Al-Sukaiti N, Al-Adawi K, Al-Riyami M, Al-Maawali A.
Mohammed M, et al.
Eur J Med Genet. 2019 Nov;62(11):103583. doi: 10.1016/j.ejmg.2018.11.017. Epub 2018 Nov 22.
Eur J Med Genet. 2019.
PMID: 30472485
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