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SPTBN5, Encoding the βV-Spectrin Protein, Leads to a Syndrome of Intellectual Disability, Developmental Delay, and

Amjad Khan1,2, Lucia Pia Bruno2,3, Fadhel Alomar4

  • 1Faculty of Science, Department of Biological Sciences (Zoology), University of Lakki Marwat, Lakki Marwat, Pakistan.

Frontiers in Molecular Neuroscience
|July 5, 2022
PubMed

Keywords:
SPTBN5heterozygous mutationintellectual disability (ID)protein modeling 3whole exome sequencing (WES)

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