A disease-causing variant in HNRNPH2 inherited from an unaffected mother with skewed X-inactivation

White‐Brown, A. M., Lemire, G., Ito, Y. A., Thornburg, O., Bain, J. M., & Dyment, D. A. (2021). A disease‐causing variant in HNRNPH2 inherited from an unaffected mother with skewed X‐inactivation. American Journal of Medical Genetics Part A, 188(2), 668–671. Portico. https://doi.org/10.1002/ajmg.a.62549
Authors:
Alexandre M White-Brown
Gabrielle Lemire
Yoko A Ito
Olivia Thornburg
Jennifer M Bain
David A Dyment
Affiliated Authors:
Olivia Thornburg
Jennifer M Bain
Subjects:
Publication Type:
Article
Unique ID:
10.1002/ajmg.a.62549
PMID:
Publication Date:
Data Source:
PubMed

Record Created: