Associated Papers
Heterozygous Pathogenic Variant in DACT1 Causes an Autosomal-Dominant Syndrome with Features Overlapping Townes-Brocks Syndrome.
Webb BD et al.
Human Mutation, 2017
Identification of novel rare mutations of DACT1 in human neural tube defects.
Shi Y et al.
Human Mutation, 2012
[A novel mutation in β-globin gene of a patient with β-thalassemia].
Peng YS et al.
Zhongguo Shi Yan Xue Ye Xue Za Zhi, 2012
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