POLG Novel Mutation with Alpers Syndrome

POLG Novel Mutation with Alpers Syndrome

Researchers at University Hospital, Berne, Switzerland describe the molecular genetic analysis of POLG in a 3.5 years old boy with VPA-induced fatal liver failure and encephalopathy (Alpers-Huttenlocher syndrome, AHS).

Bibliographic Details
Main Author: J Gordon Millichap
Format: Article
Language:English
Published: Pediatric Neurology Briefs Publishers 2012-02-01
Series:Pediatric Neurology Briefs
Subjects:
vpa-induced fatal liver failure
polg mutations
alpers syndrome
Online Access:https://www.pediatricneurologybriefs.com/articles/574
Description
Summary:Researchers at University Hospital, Berne, Switzerland describe the molecular genetic analysis of POLG in a 3.5 years old boy with VPA-induced fatal liver failure and encephalopathy (Alpers-Huttenlocher syndrome, AHS).
ISSN:1043-3155
2166-6482

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