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8q21.11 microdeletion syndrome: Delineation of HEY1 as a candidate gene in neurodevelopmental and cardiac defects.

Ikhlas Ben AyedAmal BouzidFatma KammounAmal SouissiOlfa JallouliSalma MallouliSouhir GuidaraSalma LoukilHajer AloulouFida JbeliSahar AouichaouiDorra AbidFatma AbdelhediChahnez TrikiHassen KamounSaber Masmoudi
Published in: Molecular genetics & genomic medicine (2021)
HEY1 is a candidate gene for both neurological and cardiac features of the 8q21.11 microdeletion syndrome and might, therefore, explain specific components of its pathophysiology.
Keyphrases
  • left ventricular
  • copy number
  • genome wide
  • case report
  • genome wide identification
  • dna methylation
  • genome wide analysis
  • blood brain barrier