A Further Case Supporting CCNK as a Neurodevelopmental Disease Gene


Por: Xiol-Viñas C, Olival J, Martorell-Sampol L and Ortigoza-Escobar JD

Publicada: 1 feb 2026 Ahead of Print: 1 oct 2025
Resumen:


Filiaciones:
Xiol-Viñas C:
 Department of Laboratory, Hospital Sant Joan de Déu Barcelona, Barcelona, Spain

:
 Laboratory of Neurogenetics and Molecular Medicine, Center for Genomic Sciences in Medicine, Institut de Recerca Sant Joan de Déu, Barcelona, Spain

Martorell-Sampol L:
 Department of Laboratory, Hospital Sant Joan de Déu Barcelona, Barcelona, Spain

 U-703 Centre for Biomedical Research on Rare Diseases (CIBER-ER), Instituto de Salud Carlos III, Barcelona, Spain

Ortigoza-Escobar JD:
 U-703 Centre for Biomedical Research on Rare Diseases (CIBER-ER), Instituto de Salud Carlos III, Barcelona, Spain

 European Reference Network for Rare Neurological Diseases (ERN-RND), Barcelona, Spain

 Movement Disorders Unit, Pediatric Neurology Department, Institut de Recerca, Hospital Sant Joan de Déu Barcelona, Barcelona, Spain
ISSN: 00099163





CLINICAL GENETICS
Editorial
WILEY, 111 RIVER ST, HOBOKEN 07030-5774, NJ, Dinamarca
Tipo de documento: Letter
Volumen: 109 Número: 2
Páginas: 398-399
WOS Id: 001596349400001
ID de PubMed: 41101726
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