Article info
PDFEpigenetics
Short report
CDKN1C hyperexpression in two patients with severe growth failure and microdeletions affecting the paternally inherited KCNQ1OT1:TSS-DMR
- Correspondence to Dr Masayo Kagami, Department of Molecular Endocrinology, National Research Institute for Child Health and Development, Tokyo 157-8535, Japan; kagami-ms{at}ncchd.go.jp
Citation
CDKN1C hyperexpression in two patients with severe growth failure and microdeletions affecting the paternally inherited KCNQ1OT1:TSS-DMR
Publication history
- Received May 18, 2022
- Accepted July 19, 2022
- First published July 29, 2022.
Online issue publication
November 22, 2022
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© Author(s) (or their employer(s)) 2022. No commercial re-use. See rights and permissions. Published by BMJ.