NRXN3 mutations cause developmental delay, movement disorder, and behavioral problems: CRISPR edited cells based WES results
Neda Kamal(Shiraz University of Medical Sciences), Mehdi Dianatpour(Shiraz University of Medical Sciences), Hossein Jafari Khamirani(Shiraz University of Medical Sciences), Mahintaj Dara(Shiraz University)
Cited by 21
Related Papers
Effects of short-chain fatty acid-butyrate supplementation on expression of circadian-clock genes, sleep quality, and inflammation in patients with active ulcerative colitis: a double-blind randomized controlled trial
|Lipids in Health and Disease|2024|69
A comparative in vitro and in vivo study on bone tissue engineering potential of the collagen/nano-hydroxyapatite scaffolds loaded with ginger extract and curcumin
|Materials Today Communications|2022|40
Convergence of CRISPR and artificial intelligence: A paradigm shift in biotechnology
|Human Gene|2024|28
CRISPR/Cas as a Potential Diagnosis Technique for COVID-19.
|PubMed Central|2020|26