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Label-Free Non-Linear Optics for the Study of Tubulin-Dependent Defects in Central Myelin
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A case of TUBA1A mutation presenting with lissencephaly and Hirschsprung disease

Norikatsu Hikita1, Hideji Hattori2, Mitsuhiro Kato3

  • 1Department of Pediatrics, Osaka City University Graduate School of Medicine, Osaka, Japan.

Brain & Development
|March 27, 2013
PubMed

Keywords:
Hirschsprung diseaseLissencephalyMicrocephalySyndrome of inappropriate antidiuretic hormone secretion (SIADH)TUBA1A

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