Absence of OLIG2 mutations in patients presenting with a...

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

Marie-Noelle Bonnet-Dupeyron, Patricia Combes, Odile Boespflug-Tanguy, Catherine Vaurs-Barrière
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Volume:
147B
Year:
2008
Language:
english
Pages:
2
DOI:
10.1002/ajmg.b.30613
File:
PDF, 63 KB
english, 2008
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