Functional characterization of a GFAP variant of uncertain significance in an Alexander disease case within the setting of an individualized medicine clinic.
Functional characterization of a GFAP variant of uncertain significance in an Alexander disease case within the setting of an individualized medicine clinic.
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DOI：
10.1002/ccr3.655
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发表时间：
2016-09
影响因子：
0.7
通讯作者：
Klee, Eric W
中科院分区：
文献类型：
--
作者：
Boczek, Nicole J;Sigafoos, Ashley N;Zimmermann, Michael T;Maus, Rachel L;Cousin, Margot A;Blackburn, Patrick R;Urrutia, Raul;Clark, Karl J;Patterson, Marc C;Wick, Myra J;Klee, Eric W
A de novo GFAP variant, p.R376W, was identified in a child presenting with hypotonia, developmental delay, and abnormal brain MRI. Following the 2015 ACMG variant classification guidelines and the functional studies showing protein aggregate formation in vitro, p.R376W should be classified as a pathogenic variant, causative for Alexander disease.
