Browsing by Author "Ubeyratna, N"
Now showing items 1-2 of 2
Issue Date | Title | Author(s) |
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20 May 2021 | Consolidating biallelic SDHD variants as a cause of mitochondrial complex II deficiency | Lin, S; Fasham, J; Al-Hijawi, F; et al. |
13 March 2023 | Investigation of the molecular basis of inherited neurodevelopmental disorders in Palestinian communities | Ubeyratna, N |