Clinical and molecular features of an infant patient affected by Leigh Disease associated to m.14459G > A mitochondrial DNA mutation: a case report

Title
Clinical and molecular features of an infant patient affected by Leigh Disease associated to m.14459G > A mitochondrial DNA mutation: a case report
Authors
Keywords
-
Journal
BMC Neurology
Volume 11, Issue 1, Pages -
Publisher
Springer Nature
Online
2011-07-13
DOI
10.1186/1471-2377-11-85

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