A GPHN point mutation leading to molybdenum cofactor deficiency
Article first published online: 24 OCT 2011
© 2011 John Wiley & Sons A/S
Volume 80, Issue 6, pages 598–599, December 2011
How to Cite
Reiss, J., Lenz, U., Aquaviva-Bourdain, C., Joriot-Chekaf, S., Mention-Mulliez, K. and Holder-Espinasse, M. (2011), A GPHN point mutation leading to molybdenum cofactor deficiency. Clinical Genetics, 80: 598–599. doi: 10.1111/j.1399-0004.2011.01709.x
- Issue published online: 24 OCT 2011
- Article first published online: 24 OCT 2011
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