Hereditary transthyretin amyloidosis in mainland China: a unicentric retrospective study.
Kang DuFan LiHui WangYuanfeng MiaoHe LvWei ZhangZhaoxia WangYun YuanLingchao MengPublished in: Annals of clinical and translational neurology (2021)
Chinese patients with ATTR exhibited heterogeneous TTR genotypes and clinical phenotypes. Val30Met remains the most common mutation type in mainland China.
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