Whole-genome sequencing identifies functional noncoding variation in SEMA3C that cosegregates with dyslexia in a multigenerational family

  1. Carrion-Castillo, A.
  2. Estruch, S.B.
  3. Maassen, B.
  4. Franke, B.
  5. Francks, C.
  6. Fisher, S.E.
Journal:
Human Genetics

ISSN: 1432-1203 0340-6717

Year of publication: 2021

Volume: 140

Issue: 8

Pages: 1183-1200

Type: Article

DOI: 10.1007/S00439-021-02289-W GOOGLE SCHOLAR lock_openOpen access editor

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