Identification of two novel variants of the BCL11B gene in two Chinese pedigrees associated with neurodevelopmental disorders.
Front Mol Neurosci
; 15: 927357, 2022.
Article
en En
| MEDLINE
| ID: mdl-36176959
Texto completo:
1
Banco de datos:
MEDLINE
Tipo de estudio:
Diagnostic_studies
/
Guideline
/
Prognostic_studies
/
Risk_factors_studies
Idioma:
En
Revista:
Front Mol Neurosci
Año:
2022
Tipo del documento:
Article
País de afiliación:
China