The sequencing results during the study "SEC24D depletion induces osteogenic differentiation deficiency by inactivating the ATF6/TGF-β/Runx2 regulatory loop"
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Genetic detection by whole-exome sequencing (WES) identified a novel compound heterozygous <i>SEC24D</i> variant consisting of two variants, including c.2609_2610delGA (p. R870fs*10) and c.938G>A (p. R313H) (transcript NM_014822).
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Zhang, Jing创建时间:
2024-08-14



