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Evaluation of MYORG mutations as a novel cause of primary familial brain calcification.

You ChenFeng FuSi ChenZhidong CenHaiyan TangJinxiu HuangFei XieXiaosheng ZhengDehao YangHaotian WangXuerong HuangYun ZhangYongji ZhouJing-Yu LiuWei Luo
Published in: Movement disorders : official journal of the Movement Disorder Society (2018)
We confirmed MYORG as a novel causative gene for primary familial brain calcification and further expanded the mutational and phenotypic spectrum of MYORG-related primary familial brain calcification. © 2018 International Parkinson and Movement Disorder Society.
Keyphrases
  • resting state
  • white matter
  • chronic kidney disease
  • early onset
  • functional connectivity
  • cerebral ischemia
  • multiple sclerosis
  • genome wide
  • subarachnoid hemorrhage
  • blood brain barrier