QuickView for cul7 protein human

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1. Structural and functional insights into a novel homozygous missense pathogenic variant in CUL7 ident…
2. Prenatal diagnosis and preimplantation genetics testing of 3M syndrome in a Chinese family with nove…
3. 3-M syndrome - a primordial short stature disorder with novel CUL7 mutation in two Indian patients.
4. Clinical and molecular spectrum along with genotype-phenotype correlation of 25 patients diagnosed w…
5. A novel mutation within intron 17 of the CUL7 gene results in appearance of premature termination co…

There were no clinical trials for cul7 protein human