Noonan Syndrome spectrum panels should include mutations in LZTR1 gene
Frontiers | Generation of a Mouse Model to Study the Noonan Syndrome Gene Lztr1 in the Telencephalon
LZTR1 Gene - GeneCards | LZTR1 Protein | LZTR1 Antibody
Lztr1expression in the developing telencephalon. Lztr1 gene... | Download Scientific Diagram
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 siRNA (m), shRNA and Lentiviral Particle Gene Silencers | SCBT - Santa Cruz Biotechnology
The Noonan Syndrome Gene Lztr1 Controls Cardiovascular Function by Regulating Vesicular Trafficking | Circulation Research
Mutations in LZTR1 drive human disease by dysregulating RAS ubiquitination | Science
To investigate the genetic basis in RASopathy patients | TACG
Delineation of dominant and recessive forms of LZTR1‐associated Noonan syndrome - Pagnamenta - 2019 - Clinical Genetics - Wiley Online Library
LZTR1 molecular genetic overlap with clinical implications for Noonan syndrome and schwannomatosis | BMC Medical Genomics | Full Text
LZTR1 facilitates polyubiquitination and degradation of RAS-GTPases | Cell Death & Differentiation
LZTR1 Gene - GeneCards | LZTR1 Protein | LZTR1 Antibody
Mutation of the LZTR1 gene in sporadic schwannomatosis. a From top to... | Download Scientific Diagram
The role of germline heterozygous LZTR1 variants in pediatric cancer predisposition
LZTR1 Antibodies & ELISA Kits, LZTR1 Proteins
Germline loss-of-function mutations in LZTR1 predispose to an inherited disorder of multiple schwannomas | Nature Genetics
LZTR1 is a regulator of RAS ubiquitination and signaling | Science
LZTR1-Related Hypertrophic Cardiomyopathy Without Typical Noonan Syndrome Features | Circulation: Genomic and Precision Medicine
Typical 22q11.2 deletion syndrome appears to confer a reduced risk of schwannoma | Genetics in Medicine
Providing more evidence on LZTR1 variants in Noonan syndrome patients - Chinton - 2020 - American Journal of Medical Genetics Part A - Wiley Online Library
A Chinese family with Noonan syndrome caused by a heterozygous variant in LZTR1: a case report and literature review | BMC Endocrine Disorders | Full Text
IJMS | Free Full-Text | Current Understanding of Neurofibromatosis Type 1, 2, and Schwannomatosis
