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Fenotipo clínico de una paciente con deleción de FOXP1
Clinical phenotype of a patient with FOXP1 deletion
T. Blanco Sáncheza,
, A. Duat Rodrígueza, V. Cantarín Extremeraa, P. Lapunzinab,d, M. Palomares Braloc,e, J. Nevado Blancoc,e
Corresponding author
a Servicio de Neurología, Hospital Infantil Universitario Niño Jesús, Madrid, España
b Unidad de Genética Clínica, INGEMM, Instituto de Genética Médica y Molecular, Hospital Universitario La Paz, Madrid, España
c Instituto de Investigación Sanitaria (IdiPAZ), Hospital Universitario La Paz, Madrid, España
d Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Instituto de Salud Carlos III (ISCIII), Madrid, España
e Unidad de Genómica Estructural y Funcional, INGEMM, Instituto de Genética Médica y Molecular, Hospital Universitario La Paz, Madrid, España
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