A mild clinical and neuropsychological phenotype of Renpenning syndrome: A new case report with a maternally inherited PQBP1 missense mutation
- Lopez-Martín, S.
- Albert, J.
- Peña Vila-Belda, M.D.M.
- Liu, X.
- Zhang, Z.-C.
- Han, J.
- Jiménez de Domingo, A.
- Fernández-Mayoralas, D.M.
- Fernández-Perrone, A.L.
- Calleja-Pérez, B.
- Álvarez, S.
- Fernández-Jaén, A.
ISSN: 2162-2973, 2162-2965
Année de publication: 2022
Volumen: 11
Número: 4
Pages: 921-927
Type: Article