Kaifeng Zheng
Shenzhen, 518040, China
Last Updated: 09/26/2026
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Found 9 publications
NAALAD2 mutations disrupt the fate of photoreceptor cells and retinal pigment epithelial cells during early retinal development.
Journal: Pharmacological research
Published: December 14, 2024
Deficiency in the conserved ECHS1 gene causes Leigh syndrome by impairing mitochondrial respiration efficiency and suppressing ADRB2-PKA signaling.
Journal: Biochimica et biophysica acta. Molecular basis of disease
Published: September 10, 2024
Novel compound heterozygous MYO15A splicing variants in autosomal recessive non-syndromic hearing loss.
Journal: BMC medical genomics
Published: August 25, 2023
Reduction of Missed Diagnosis of G6PD Deficiency in Heterozygous Females by G6PD/6PGD Ratio Assay Combined with Amplification Refractory Mutation System PCR.
Journal: Human heredity
Published: March 03, 2022
Assessment of the association between the polymorphism rs1256031 of the estrogen receptor β gene and GDM susceptibility.
Journal: Nagoya journal of medical science
Published: December 14, 2020
Leber's Hereditary Optic Neuropathy-Specific Heteroplasmic Mutation m.14495A>G Found in a Chinese Family.
Journal: Translational vision science & technology
Published: October 01, 2018
A Novel Potentially Causative Variant of NDUFAF7 Revealed by Mutation Screening in a Chinese Family With Pathologic Myopia.
Journal: Investigative ophthalmology & visual science
Published: August 25, 2017
Exome sequencing identifies a novel mutation of the GDI1 gene in a Chinese non-syndromic X-linked intellectual disability family.
Journal: Genetics and molecular biology
Published: September 18, 2016
Showing 1-9 of 9
Last Updated: 09/26/2026