Mitochondrial dysfunction in Stüve-Wiedemann syndrome in a patient carrying an ND1 gene mutation [4]

Eva Morava; Ben Hamel; Frans Hol; Richard Rodenburg; Jan Smeitink

doi:10.1002/ajmg.a.31452

Mitochondrial dysfunction in Stüve-Wiedemann syndrome in a patient carrying an ND1 gene mutation [4]

Eva Morava, Ben Hamel, Frans Hol, Richard Rodenburg, Jan Smeitink

Medical Genetics

Research output: Contribution to journal › Letter › peer-review

9 Scopus citations

Original language	English (US)
Pages (from-to)	2248-2250
Number of pages	3
Journal	American Journal of Medical Genetics, Part A
Volume	140
Issue number	20
DOIs	https://doi.org/10.1002/ajmg.a.31452
State	Published - Oct 15 2006

ASJC Scopus subject areas

Genetics
Genetics(clinical)

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10.1002/ajmg.a.31452

Cite this

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title = "Mitochondrial dysfunction in St{\"u}ve-Wiedemann syndrome in a patient carrying an ND1 gene mutation [4]",

author = "Eva Morava and Ben Hamel and Frans Hol and Richard Rodenburg and Jan Smeitink",

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AU - Morava, Eva

AU - Hamel, Ben

AU - Hol, Frans

AU - Rodenburg, Richard

AU - Smeitink, Jan

PY - 2006/10/15

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AN - SCOPUS:33749465506

SN - 1552-4825

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JO - American Journal of Medical Genetics, Part A

JF - American Journal of Medical Genetics, Part A

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ER -

Mitochondrial dysfunction in Stüve-Wiedemann syndrome in a patient carrying an ND1 gene mutation [4]

ASJC Scopus subject areas

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