Name : Recombinant Human ARL6IP6 Protein (mFc Tag) Biological Activity : Background : It had been found that a homozygous truncating mutation in ARL6IP6 as the likely cause of a syndromic form of CMTC associated with major dysmorphism, developmental delay, transient ischemic attacks and cerebral vascular malformations. This gene was previously implicated by genome wide association study …
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