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Does the Co-occurrence of FGFR3 Gene Mutation in Hypochondroplasia, Medial Temporal Lobe Dysgenesis, and Focal Epilepsy Suggest a Syndrome?
Romeo, Antonino, Lodi, Monica, Viri, Maurizio, Parente, Eliana, Baldi, Maurizia, Righini, Andrea, Milani, DonatellaVolume:
50
Language:
english
Journal:
Pediatric Neurology
DOI:
10.1016/j.pediatrneurol.2014.01.004
Date:
April, 2014
File:
PDF, 861 KB
english, 2014