Neurodevelopmental disorders and the mystery of the genes involved: a case report of a bicra heterozygous mutation identified in autism spectrum disorder

HIGHLIGHTS

• What: This case highlights the complexity of neurodevelopmental disorders and the importance of further understanding their underlying mechanisms.
• Who: CC-BY et al. from the Pediatrics, Centro Medico Episcopal San Lucas, Ponce, PRI Pediatrics, Ponce Health Sciences University, Ponce have published the Article: Review began 07/21/2024 Review ended 08/04/2024 Published 08/08/2024 © Copyright, in the Journal: (JOURNAL) of August/08,/2024
• How: A post-natal oligonucleotide single nucleotide polymorphism (SNP) chromosomal microarray was conducted to explore the patient`s developmental disorder presentation.
• Future: Research is crucial . . .
  

   

  

  If you want to have access to all the content you need to log in!

  Thanks :)

  Username or E-mail:

  If you don't have an account, you can create one here.