Associated Papers
The implication of holocytochrome c synthase mutation in Korean familial hypoplastic amelogenesis imperfecta.
Choi H et al.
Clinical Oral Investigations, 2022
Identification of potential causal variants for premature ovarian failure by whole exome sequencing.
Jin H et al.
Bmc Medical Genomics, 2020
33109206 (PubMed )
Supplement: 12920_2020_813_MOESM1_ESM.xlsx › Table_S4
Genomic analysis identifies masqueraders of full-term cerebral palsy.
Takezawa Y et al.
Annals of Clinical and Translational Neurology, 2018
29761117 (PubMed )
Supplement: ACN3-5-538-s001.xlsx › Sheet1
Identification of EGFLAM, SPATC1L and RNASE13 as novel susceptibility loci for aortic aneurysm in Japanese individuals by exome-wide association studies.
Yamada Y et al.
International Journal of Molecular Medicine, 2017
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