Does the Co-occurrence of FGFR3 Gene Mutation in Hypochondroplasia, Medial Temporal Lobe Dysgenesis, and Focal Epilepsy Suggest a Syndrome?

✍ Scribed by Romeo, Antonino; Lodi, Monica; Viri, Maurizio; Parente, Eliana; Baldi, Maurizia; Righini, Andrea; Milani, Donatella

• Book ID: 122226521
• Publisher: Elsevier Science
• Year: 2014
• Tongue: English
• Weight: 861 KB
• Volume: 50
• Category: Article
• ISSN: 0887-8994
• DOI: 10.1016/j.pediatrneurol.2014.01.004