Browsing by Author "Al-Salmi, F"
Now showing items 1-3 of 3
Issue Date | Title | Author(s) |
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1 June 2021 | Investigation of the molecular basis of inherited neurological conditions in Oman | Al-Salmi, F |
3 January 2017 | A mutation of EPT1 (SELENOI) underlies a new disorder of Kennedy pathway phospholipid biosynthesis | Ahmed, MY; Al-Khayat, A; Al-Murshedi, F; et al. |
28 February 2017 | PRUNE is crucial for normal brain development and mutated in microcephaly with neurodevelopmental impairment | Zollo, M; Ahmed, M; Ferrucci, V; et al. |