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ZFHX3
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Haploinsufficiency of ZFHX3, encoding a key player in neuronal development, causes syndromic intelle…
Exonic trinucleotide repeat expansions in ZFHX3 cause spinocerebellar ataxia type 4: A poly-glycine …
Myeloid Zfhx3 deficiency protects against hypercapnia-induced suppression of host defense against in…
Loss of the Atrial Fibrillation-Related Gene, Zfhx3, Results in Atrial Dilation and Arrhythmias.
Adaptive Long-Read Sequencing Reveals GGC Repeat Expansion in ZFHX3 Associated with Spinocerebellar …
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Detection of Occult Paroxysmal AF in Cryptogenic Stroke or TIA Patients Using an Implantable Loop Re…
Pharmacogenetic Study of Antiarrhythmic Drugs for Atrial Fibrillation
Analysis of Androgene Receptors Axis and DNA Damage Repair Genes in Patients With Prostate Cancer
Study to Evaluate ctDNA of mCSPC Patients Receiving Apalutamide in Japan
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