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Brain monoamine vesicular transport disease caused by homozygous SLC18A2 variants: A study in 42 affected individuals.
Genet Med. 2023 Jan;25(1):90-102. doi: 10.1016/j.gim.2022.09.010. Epub 2022 Oct 31.
Genet Med. 2023.
PMID: 36318270
Free article.
Mutational and bioinformatics analysis of the NKX2.1 gene in a cohort of Iranian pediatric patients with congenital hypothyroidism (CH).
Heidari MM, Madani Manshadi SA, Eshghi AR, Talebi F, Khatami M, Bragança J, Ordooei M, Chamani R, Ghasemi F.
Heidari MM, et al. Among authors: madani manshadi sa.
Physiol Int. 2022 Jun 7;109(2):261-277. doi: 10.1556/2060.2022.00224. Print 2022 Jun 16.
Physiol Int. 2022.
PMID: 35895569
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