Biallelic deletion in a minimal CAPN15 intron in siblings with a recognizable syndrome of congenital malformations and developmental delay.

Biallelic deletion in a minimal CAPN15 intron in siblings with a recognizable syndrome of congenital malformations and developmental delay. Clin Genet. 2021 Jan 07;: Authors: Mor-Shaked H, Salah S, Yanovsky-Dagan S, Meiner V, Atawneh OM, Abu-Libdeh B, Elpeleg O, Harel T PMID: 33410501 [PubMed - as supplied by publisher]

https://www.ncbi.nlm.nih.gov/pubmed/33410501?dopt=Abstract

Source: Clinical Genetics - January 7, 2021 Category: Genetics & Stem Cells Authors: Mor-Shaked H, Salah S, Yanovsky-Dagan S, Meiner V, Atawneh OM, Abu-Libdeh B, Elpeleg O, Harel T Tags: Clin Genet Source Type: research

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