A mutation in PEX19 causes a severe clinical phenotype in a patient with peroxisomal biogenesis disorder (Q55053133)
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scientific article published on September 1, 2010
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | A mutation in PEX19 causes a severe clinical phenotype in a patient with peroxisomal biogenesis disorder |
scientific article published on September 1, 2010 |
Statements
A mutation in PEX19 causes a severe clinical phenotype in a patient with peroxisomal biogenesis disorder (English)
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Ronald J A Wanders
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Merel S. Ebberink
Hans R. Waterham
Sarar Mohamed
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Ebtisam El-Meleagy
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Abdelhaleem Nasr
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1 September 2010
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152A
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9
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2318-2321
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