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Homozygous Missense Variant F12 (Gly506Asp) Associated With Severe Factor XII Deficiency: A case Report
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Title: Figure 3 from novel homozygous adamts17 missense variant in weillFigure 3 from novel homozygous adamts17 missense variant in weill.
Title: (pdf) homozygous missense variant f12 (gly506asp) associated with(pdf) homozygous missense variant f12 (gly506asp) associated with.
Title: Homozygous missense variant in popdc3 causes recessive limb‐girdleHomozygous missense variant in popdc3 causes recessive limb‐girdle.
