https://mptpchemical.com/the-a....daptive-rating-syste
Clinical Trial Registration Number CTRI/2019/03/018239 registered on March 25, 2019.Sneddon problem is an uncommon condition impacting little and medium sized bloodstream that is characterized by the organization of livedo reticularis and stroke. We performed whole-exome sequencing (WES) in 2 affected siblings of a consanguineous family with childhood-onset stroke and identified a homozygous nonsense mutation in the epidermal development aspect repeat (EGFr) 19 of NOTCH3, p.(Arg735Ter). WES of 6 additional instances
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