A novel stop codon variant affecting ΔNp63 isoforms associated with non-syndromic limb-mammary phenotype and uterine cervix dysplasia.

A novel stop codon variant affecting ΔNp63 isoforms associated with non-syndromic limb-mammary phenotype and uterine cervix dysplasia. Clin Genet. 2020 Dec 01;: Authors: Guazzarotti L, Sani I, Giglio S, Brunello F, Perilongo G, Bocciardi R PMID: 33258108 [PubMed - as supplied by publisher]

https://www.ncbi.nlm.nih.gov/pubmed/33258108?dopt=Abstract

Source: Clinical Genetics - December 1, 2020 Category: Genetics & Stem Cells Authors: Guazzarotti L, Sani I, Giglio S, Brunello F, Perilongo G, Bocciardi R Tags: Clin Genet Source Type: research

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