Loss-of-function mutations in MICU1 cause a brain and muscle disorder linked to primary alterations in mitochondrial calcium signaling

Những quyển sách tương tự

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  Được phát hành: (2013)
• Variable expressivity of ciliopathy neurological phenotypes that encompass Meckel–Gruber syndrome and Joubert syndrome is caused by complex de-regulated ciliogenesis, Shh and Wnt signalling defects
  Bằng: Zakia A. Abdelhamed, et al.
  Được phát hành: (2013)