50 Years Ago in TheJournalofPediatrics: Unique X-Linked Mutation Associated with Female-Specific Epilepsy and Intellectual Disability

J Pediatr. 2021 Nov:238:144. doi: 10.1016/j.jpeds.2021.08.047.

Authors

Mark D Orland¹, Philip F Giampietro²

Affiliations

¹ College of Medicine, University of Illinois-Chicago.
² Professor of Pediatrics, Division of Medical Genetics, University of Illinois-Chicago, Department of Pediatrics, Chicago, Illinois.

PMID: 34702493
DOI: 10.1016/j.jpeds.2021.08.047

No abstract available

MeSH terms

Cadherins / genetics
Epilepsy / complications
Epilepsy / genetics*
Female
Genes, X-Linked
Humans
Intellectual Disability / complications
Intellectual Disability / genetics*
Mutation
Protocadherins

Substances

Cadherins
PCDH19 protein, human
Protocadherins