Articles with "variant 5457" as a keyword



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Biallelic deep intronic variant c.5457+81T>A in TRIP11 causes loss of function and results in achondrogenesis 1A

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Published in 2021 at "Human Mutation"

DOI: 10.1002/humu.24235

Abstract: Biallelic loss of function variants in TRIP11 encoding for the Golgi microtubule‐associated protein 210 (GMAP‐210) causes the lethal chondrodysplasia achondrogenesis type 1A (ACG1A). Loss of TRIP11 activity has been shown to impair Golgi structure, vesicular… read more here.

Keywords: 5457 81t; deep intronic; variant 5457; variant ... See more keywords