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Identification of a novel LATS1 variant associated with familial cerebral cavernous malformations in a Chinese family.

Liangyuan GengTao JiangYihao ZhuQingru WangWenwen YuanXinhua HuYuanjie ZouHong XiaoHongyi Liu
Published in: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology (2022)
Our findings indicated that the LATS1 variant could be a potential pathogenic factor for FCCMs in this Chinese family.
Keyphrases
  • subarachnoid hemorrhage
  • early onset