Epileptic phenotype of FGFR3-related bilateral medial temporal lobe dysgenesis-Reference-Cited by-同舟云学术

Epileptic phenotype of FGFR3-related bilateral medial temporal lobe dysgenesis

Published:2017-01 Issue:1 Volume:39 Page:67-71
ISSN:0387-7604
Container-title:Brain and Development
language:en
Short-container-title:Brain and Development

Author:

Okazaki Tetsuya,Saito Yoshiaki,Ueda Riyo,Awashima Takeya,Nishimura Yoko,Yuasa Isao,Shinohara Yuki,Adachi Kaori,Sasaki Masayuki,Nanba Eiji,Maegaki Yoshihiro

Publisher

Elsevier BV

Subject

Clinical Neurology,Developmental Neuroscience,General Medicine,Pediatrics, Perinatology, and Child Health

Reference9 articles.

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3. Does the co-occurrence of FGFR3 gene mutation in hypochondroplasia, medial temporal lobe dysgenesis, and focal epilepsy suggest a syndrome?;Romeo;Pediatr Neurol,2014

4. High specificity of head circumference to recognize N540K mutation in hypochondroplasia;Fano;Ann Hum Biol,2005

5. Medial temporal lobe dysgenesis in hypochondroplasia;Kannu;Am J Med Genet A,2005

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