A Brazilian case arising from a homozygous canonical splice site SLC35A3 variant leading in-frame deletion.

A Brazilian case arising from a homozygous canonical splice site SLC35A3 variant leading in-frame deletion. Clin Genet. 2021 Jan 08;: Authors: Miyake N, de Oliveira Stephan B, Kim CA, Matsumoto N PMID: 33416188 [PubMed - as supplied by publisher]

https://www.ncbi.nlm.nih.gov/pubmed/33416188?dopt=Abstract

Source: Clinical Genetics - January 8, 2021 Category: Genetics & Stem Cells Authors: Miyake N, de Oliveira Stephan B, Kim CA, Matsumoto N Tags: Clin Genet Source Type: research

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