Article info

Findings that shed new light on the possible pathogenesis of a disease or an adverse effect
A novel mitochondrial ATP8 gene mutation in a patient with apical hypertrophic cardiomyopathy and neuropathy
  1. j.smeitink{at}cukz.umcn.nl
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Citation

Jonckheere AI, Hogeveen M, Nijtmans L, et al
A novel mitochondrial ATP8 gene mutation in a patient with apical hypertrophic cardiomyopathy and neuropathy

Publication history

  • First published January 23, 2009.
Online issue publication 
August 07, 2018

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