Further evidence that DDHD2...

European Journal of Neurology 2014 / 03 Vol. 21; Iss. 3

Further evidence that DDHD2 gene mutations cause autosomal recessive hereditary spastic paraplegia with thin corpus callosum

Magariello, A., Citrigno, L., Zuchner, S., Gonzalez, M., Patitucci, A., Sofia, V., Conforti, F. L., Pappalardo, I., Mazzei, R., Ungaro, C., Zappia, M., Muglia, M.
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Volume:
21
Language:
english
Journal:
European Journal of Neurology
DOI:
10.1111/ene.12305
Date:
March, 2014
File:
PDF, 532 KB
english, 2014
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