Genetic Polymorphisms in ZFHX3 Are Associated with Atrial Fibrillation in a Chinese Han Population
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Publisher
Public Library of Science (PLoS)
Subject
Multidisciplinary
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1. Spinocerebellar ataxia type 4 is caused by a GGC expansion in the ZFHX3 gene and is associated with prominent dysautonomia and motor neuron signs;Journal of Internal Medicine;2024-07-07
2. Haploinsufficiency of ZFHX3, encoding a key player in neuronal development, causes syndromic intellectual disability;The American Journal of Human Genetics;2024-03
3. Risk stratification of atrial fibrillation and stroke using single nucleotide polymorphism and circulating biomarkers;PLOS ONE;2023-10-12
4. Spinocerebellar ataxia type 4 is caused by a GGC expansion in theZFHX3gene and is associated with prominent dysautonomia and motor neuron signs;2023-10-03
5. A novel neurodevelopmental syndrome caused by loss-of-function of the Zinc Finger Homeobox 3 (ZFHX3) gene;2023-05-24
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