Five new cases of syndromic intellectual disability due to KAT6A mutations: widening the molecular and clinical spectrum
16 auth.
R. Urreizti,
Estrella López-Martín,
A. Martínez-Monseny,
Montse Pujadas,
Laura Castilla-Vallmanya,
L. Pérez-Jurado,
M. Serrano,
D. Natera-de Benito,
B. Martínez-Delgado,
M. Posada-de-la-Paz,
...
J. Alonso,
Purificación Marín-Reina,
M. O’Callaghan,
D. Grinberg,
E. Bermejo-Sánchez,
S. Balcells
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4 |
2020 |
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