LZTR1 Gene - GeneCards | LZTR1 Protein | LZTR1 Antibody
Genes | Free Full-Text | Simultaneous Detection of NF1, SPRED1, LZTR1, and NF2 Gene Mutations by Targeted NGS in an Italian Cohort of Suspected NF1 Patients
LZTR1 is a regulator of RAS ubiquitination and signaling | Science
Further Evidence for the Implication of LZTR1, a Gene not Associated with the Ras-Mapk Pathway, in the Pathogenesis of Noonan Syndrome | Semantic Scholar
![PDF] Dominant Noonan syndrome-causing LZTR1 mutations specifically affect the Kelch domain substrate-recognition surface and enhance RAS-MAPK signaling | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/c5076789ebfec6246d433c911f984be32d2b239c/11-Figure8-1.png "PDF] Dominant Noonan syndrome-causing LZTR1 mutations specifically affect the Kelch domain substrate-recognition surface and enhance RAS-MAPK signaling | Semantic Scholar")
PDF] Dominant Noonan syndrome-causing LZTR1 mutations specifically affect the Kelch domain substrate-recognition surface and enhance RAS-MAPK signaling | Semantic Scholar
Providing more evidence on LZTR1 variants in Noonan syndrome patients - Chinton - 2020 - American Journal of Medical Genetics Part A - Wiley Online Library
Mutations in LZTR1 drive human disease by dysregulating RAS ubiquitination | Science
Expanding the mutational spectrum of LZTR1 in schwannomatosis | European Journal of Human Genetics
To investigate the genetic basis in RASopathy patients | TACG
LZTR1 inactivation promotes MAPK/ ERK pathway activation in glioblastoma by stabilizing oncoprotein RIT1 | bioRxiv
A Chinese family with Noonan syndrome caused by a heterozygous variant in LZTR1: a case report and literature review | BMC Endocrine Disorders | Full Text
The role of germline heterozygous LZTR1 variants in pediatric cancer predisposition
Rare variants in SOS2 and LZTR1 are associated with Noonan syndrome | Journal of Medical Genetics
Biomolecules | Free Full-Text | Exome Survey and Candidate Gene Re-Sequencing Identifies Novel Exstrophy Candidate Genes and Implicates LZTR1 in Disease Formation
Schematic structure of LZTR1 mutations or variants identified to date.... | Download Scientific Diagram
Comprehensive mutation analysis of all three genes, LZTR1, SMARCB1, and... | Download Scientific Diagram
LZTR1-Related Hypertrophic Cardiomyopathy Without Typical Noonan Syndrome Features | Circulation: Genomic and Precision Medicine
Cross-species analysis of LZTR1 loss-of-function mutants demonstrates dependency to RIT1 orthologs | eLife
Typical 22q11.2 deletion syndrome appears to confer a reduced risk of schwannoma | Genetics in Medicine
Germline loss-of-function mutations in LZTR1 predispose to an inherited disorder of multiple schwannomas | Nature Genetics
Mutation of the LZTR1 gene in sporadic schwannomatosis. a From top to... | Download Scientific Diagram
Noonan Syndrome spectrum panels should include mutations in LZTR1 gene
LZTR1 Gene - GeneCards | LZTR1 Protein | LZTR1 Antibody
Germline loss-of-function mutations in LZTR1 predispose to an inherited disorder of multiple schwannomas | Nature Genetics
