共 50 条
- [32] A Novel Heterozygous Missense Variant in the LZTR1 Gene as a cause of Noonan Syndrome HORMONE RESEARCH IN PAEDIATRICS, 2018, 90 : 446 - 446
- [37] LZTR1 molecular genetic overlap with clinical implications for Noonan syndrome and schwannomatosis BMC Medical Genomics, 15