Expanding the Phenotypic Spectrum and Variability of Endocrine Abnormalities Associated With TUBB3 E410K Syndrome

Lignende værker

• Altered White Matter Organization in the TUBB3 E410K Syndrome
  af: Grant, P Ellen, et al.
  Udgivet: (2019)
• A novel syndrome caused by the E410K amino acid substitution in the neuronal β-tubulin isotype 3
  af: Chew, Sheena, et al.
  Udgivet: (2013)
• Expanding the phenotypic spectrum of ECEL1-related congenital contracture syndromes
  af: Shaaban, Sherin, et al.
  Udgivet: (2013)
• Expanding the Spectrum of Founder Mutations Causing Isolated Gonadotropin-Releasing Hormone Deficiency
  af: Choi, Jin-Ho, et al.
  Udgivet: (2015)
• Two Unique TUBB3 Mutations Cause Both CFEOM3 and Malformations of Cortical Development
  af: Whitman, Mary C., et al.
  Udgivet: (2015)