Supplemental Table 1 Genotypic and phenotypic characteristics of patients with CNKSR2 gene mutation causing MRXHG as reported in previous literature
Abstract
The table summarizes the genotypic and phenotypic characteristics of patients with MRXHG associated with CNKSR2 gene mutations.
Fields of Study & Subjects
Genomics and Rare Diseases
Genetics and Neurodevelopmental Disorders
Immunodeficiency and Autoimmune Disorders
Publication details
- Journal / source
- ScienceDB
- Publication date
- 2 March 2026
- Language
- ZH