Author response for 'A novel bi‐allelic loss‐of‐function mutation in STIM1 expands the phenotype of STIM1 ‐related diseases'

Autor:	J. Andoni Urtizberea, Nicolas Lévy, Catherine Robert, Moiz Bakhiet, Valérie Delague, Marc Bartoli, Alexandra Salvi, Nathalie Da Silva, André Mégarbané, Cristina Skrypnyk
Rok vydání:	2021
Předmět:	Genetics Mutation (genetic algorithm) STIM1 Biology Phenotype Allelic loss Function (biology)
DOI:	10.1111/cge.13959/v3/response1
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c1ec89e01ba6cf0786a986d410abf100 https://doi.org/10.1111/cge.13959/v3/response1 Zobrazit plný text záznamu