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Absence of OLIG2 mutations in patients presenting with a severe Pelizaeus-Merzbacher-like leukodystrophy associated with motor neuron dysfunction

✍ Scribed by Marie-Noelle Bonnet-Dupeyron; Patricia Combes; Odile Boespflug-Tanguy; Catherine Vaurs-Barrière


Publisher
John Wiley and Sons
Year
2008
Tongue
English
Weight
63 KB
Volume
147B
Category
Article
ISSN
1552-4841

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