Further Evidence for the Implication of LZTR1, a Gene not Associated with the Ras-Mapk Pathway, in the Pathogenesis of Noonan Syndrome | Semantic Scholar
LZTR1 Gene - GeneCards | LZTR1 Protein | LZTR1 Antibody
Mutations in LZTR1 drive human disease by dysregulating RAS ubiquitination | Science
Cross-species analysis of LZTR1 loss-of-function mutants demonstrates dependency to RIT1 orthologs | eLife
Rare variants in SOS2 and LZTR1 are associated with Noonan syndrome | Journal of Medical Genetics
The Noonan Syndrome Gene Lztr1 Controls Cardiovascular Function by Regulating Vesicular Trafficking | Circulation Research
Typical 22q11.2 deletion syndrome appears to confer a reduced risk of schwannoma | Genetics in Medicine
The Noonan Syndrome Gene Lztr1 Controls Cardiovascular Function by Regulating Vesicular Trafficking | Circulation Research
LZTR1: A promising adaptor of the CUL3 family (Review)
The Noonan Syndrome Gene Lztr1 Controls Cardiovascular Function by Regulating Vesicular Trafficking | Circulation Research
To investigate the genetic basis in RASopathy patients | TACG
LZTR1 inactivation promotes MAPK/ ERK pathway activation in glioblastoma by stabilizing oncoprotein RIT1 | bioRxiv
Expanding the mutational spectrum of LZTR1 in schwannomatosis | European Journal of Human Genetics
Delineation of dominant and recessive forms of LZTR1‐associated Noonan syndrome - Pagnamenta - 2019 - Clinical Genetics - Wiley Online Library
Biomolecules | Free Full-Text | Exome Survey and Candidate Gene Re-Sequencing Identifies Novel Exstrophy Candidate Genes and Implicates LZTR1 in Disease Formation
Mutation of the LZTR1 gene in sporadic schwannomatosis. a From top to... | Download Scientific Diagram
LZTR1 Antibodies & ELISA Kits, LZTR1 Proteins
Lztr1expression in the developing telencephalon. Lztr1 gene... | Download Scientific Diagram
LZTR1 molecular genetic overlap with clinical implications for Noonan syndrome and schwannomatosis | BMC Medical Genomics | Full Text
LZTR1 inactivation promotes MAPK/ ERK pathway activation in glioblastoma by stabilizing oncoprotein RIT1 | bioRxiv
LZTR1-Related Hypertrophic Cardiomyopathy Without Typical Noonan Syndrome Features | Circulation: Genomic and Precision Medicine
LZTR1 facilitates polyubiquitination and degradation of RAS-GTPases | Cell Death & Differentiation
The role of germline heterozygous LZTR1 variants in pediatric cancer predisposition
Noonan Syndrome spectrum panels should include mutations in LZTR1 gene
