Mitochondrial dysfunction in Stüve-Wiedemann syndrome in a patient carrying an ND1 gene mutation.
作者信息
Morava Eva, Hamel Ben, Hol Frans, Rodenburg Richard, Smeitink Jan
机构信息
Department of Pediatrics, Nijmegen Centre for Mitochondrial Disorders, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands.
出版信息
Am J Med Genet A. 2006 Oct 15;140(20):2248-50. doi: 10.1002/ajmg.a.31452.
PMID:16969869
Abstract
摘要
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