Records containing: Microcephalic Osteodysplastic Primordial Dwarfism Types I and III

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CLINICAL_TRIALS study record update · 2024-10-09
Study of the Consequences of Mutations of the RNU4ATAC and RTTN Genes by Transcriptomic, Biochemical and Cellular Approaches in Order to Determine the Pathophysiology of Their Associated Syndromes: Microcephalic Osteodysplastic Primordial Dwarfism Type I/III, Roifman Syndrome and Lowry-Wood Syndrome