Associated Papers
Missense mutation of NRAS is associated with malignant progression in neurocutaneous melanosis.
Takahashi H et al.
Acta Neuropathologica Communications, 2024
Identification of biallelic variations of CEP70 in patients with male infertility.
Ruan T et al.
Frontiers in Endocrinology, 2023
36967801 (PubMed )
Supplement: Table_1.xlsx › Patient_1
Integrated genomic analysis reveals mutated ELF3 as a potential gallbladder cancer vaccine candidate.
Pandey A et al.
Nature Communications, 2020
32839463 (PubMed )
Supplement: 41467_2020_17880_MOESM8_ESM.xlsx › GBC_Cell_LIne_Mutations
A rare variant in the FHL1 gene associated with X-linked recessive hypoparathyroidism.
Pillar N et al.
Human Genetics, 2017
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