Germline loss-of-function mutations in LZTR1 predispose to an inherited disorder of multiple schwannomas | Nature Genetics
Biomolecules | Free Full-Text | Exome Survey and Candidate Gene Re-Sequencing Identifies Novel Exstrophy Candidate Genes and Implicates LZTR1 in Disease Formation
A Chinese family with Noonan syndrome caused by a heterozygous variant in LZTR1: a case report and literature review | BMC Endocrine Disorders | Full Text
LZTR1 Gene - GeneCards | LZTR1 Protein | LZTR1 Antibody
Mutations in LZTR1 drive human disease by dysregulating RAS ubiquitination | Science
Germline loss-of-function mutations in LZTR1 predispose to an inherited disorder of multiple schwannomas | Nature Genetics
LZTR1 inactivation promotes MAPK/ ERK pathway activation in glioblastoma by stabilizing oncoprotein RIT1 | bioRxiv
Comprehensive mutation analysis of all three genes, LZTR1, SMARCB1, and... | Download Scientific Diagram
To investigate the genetic basis in RASopathy patients | TACG
The Noonan Syndrome Gene Lztr1 Controls Cardiovascular Function by Regulating Vesicular Trafficking | Circulation Research
LZTR1 molecular genetic overlap with clinical implications for Noonan syndrome and schwannomatosis | BMC Medical Genomics | Full Text
Providing more evidence on LZTR1 variants in Noonan syndrome patients - Chinton - 2020 - American Journal of Medical Genetics Part A - Wiley Online Library
LZTR1-Related Hypertrophic Cardiomyopathy Without Typical Noonan Syndrome Features | Circulation: Genomic and Precision Medicine
Frontiers | Generation of a Mouse Model to Study the Noonan Syndrome Gene Lztr1 in the Telencephalon
Typical 22q11.2 deletion syndrome appears to confer a reduced risk of schwannoma | Genetics in Medicine
LZTR1 Gene - GeneCards | LZTR1 Protein | LZTR1 Antibody
Further Evidence for the Implication of LZTR1, a Gene not Associated with the Ras-Mapk Pathway, in the Pathogenesis of Noonan Syndrome | Semantic Scholar
The Noonan Syndrome Gene Lztr1 Controls Cardiovascular Function by Regulating Vesicular Trafficking | Circulation Research
Delineation of LZTR1 mutation-positive patients with Noonan syndrome and identification of LZTR1 binding to RAF1–PPP1CB complexes | SpringerLink
Noonan Syndrome spectrum panels should include mutations in LZTR1 gene
Mutation of the LZTR1 gene in sporadic schwannomatosis. a From top to... | Download Scientific Diagram
Mutations in LZTR1 drive human disease by dysregulating RAS ubiquitination – Science Mission
