View in EDS

Patient with a heterozygous pathogenic variant in CSNK2A1 gene: A new case to update the Okur–Chung neurodevelopmental syndrome.

Saved in:

Bibliographic Details
Title:	Patient with a heterozygous pathogenic variant in CSNK2A1 gene: A new case to update the Okur–Chung neurodevelopmental syndrome.
Authors:	Blanc, Albin¹, albin.blanc@gmail.com, Bonnet, Céline^2,3, Wandzel, Marion², Roth, Virginie², Duffourd, Yannis^4,5, Safraou, Hanna^4,5, Leheup, Bruno³, Muller, Florence⁶, D Colne, Julie⁷, Feillet, François^3,8, Schmitt, Emmanuelle⁹, Castro, Matheus^10,11, Savatt, Jullian¹², Burcheri, Adriano¹³, Nemos, Christophe^14,15,16,17, Philippe, Christophe^4,5, Lambert, Laëtitia^1,3
Source:	American Journal of Medical Genetics. Part A; Sep2024, Vol. 194 Issue 9, p1-6, 6p
Database:	Applied Science & Technology Source

Description
ISSN:	15524825
DOI:	10.1002/ajmg.a.63642