Open AccessExploring the role of LZTR1 in an autosomal recessive form of Noonan Syndrome by genome-edited induced pluripotent stem cells
Author(s) -
AUTHOR_ID,
Robin Hindmarsh
Publication year - 2022
Language(s) - English
Resource type - Dissertations/theses
DOI - 10.53846/goediss-8838
Subject(s) - noonan syndrome , exome , exome sequencing , costello syndrome , genetics , short stature , medicine , mutation , biology , pediatrics , gene , kras