RevNeurol
 2016
DOI: 10.33588/rn.6205.2015380
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Paraplejía espástica hereditaria ligada al cromosoma X por mutación en el gen L1CAM: presentación de tres casos del síndrome CRASH

Arturo Muñoz
1
,
Cabrera-López Jc
2
,
Alfredo Rodriguez
3
et al.
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