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NRXN3 mutations cause developmental delay, movement disorder, and behavioral problems: CRISPR edited cells based WES results.
Kamal, Neda; Jafari Khamirani, Hossein; Dara, Mahintaj; Dianatpour, Mehdi.
Affiliation
  • Kamal N; Department of Medical Genetics, Shiraz University of Medical Sciences, Shiraz, Iran.
  • Jafari Khamirani H; Department of Medical Genetics, Shiraz University of Medical Sciences, Shiraz, Iran.
  • Dara M; Stem Cells Technology Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.
  • Dianatpour M; Department of Medical Genetics, Shiraz University of Medical Sciences, Shiraz, Iran; Stem Cells Technology Research Center, Shiraz University of Medical Sciences, Shiraz, Iran. Electronic address: mdianatpur@gmail.com.
Gene ; 867: 147347, 2023 May 30.
Article in En | MEDLINE | ID: mdl-36898513
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Intellectual Disability / Movement Disorders Limits: Animals Country/Region as subject: Asia Language: En Journal: Gene Year: 2023 Document type: Article Affiliation country: Irán Country of publication: Países Bajos
Fulltext
Add to My VHL
Print
XML
PubMed Links
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Intellectual Disability / Movement Disorders Limits: Animals Country/Region as subject: Asia Language: En Journal: Gene Year: 2023 Document type: Article Affiliation country: Irán Country of publication: Países Bajos