Insight into Genetic Mutations of SZT2: Is It a Syndrome?

Osama Yousef MuthaffarMohammed M S JanAnas S Alyazidi Taif K AlotibiEman A Alsulami

Published in: Biomedicines (2023)

mutations. High variability among the cases was observed. Developmental delay and facial dysmorphism can be investigated as potential hallmarks; aiding clinicians in diagnosing the condition and optimizing management plans.

Keyphrases

health insurance
case report
atomic force microscopy
copy number
human health
gene expression
mass spectrometry
dna methylation