Analysis through exome sequencing in patients with non familial primary congenital cataract


Por: Messina-Baas, O. M., Leon-Oviedo, C., Valdes-Miranda, J. M., Rivera-Vega, M. R., Vega-Gama, R., Xilotl-DeJesus, N., Martinez-Montoya, V., Tovar-Ayala, M. G., Gonzalez-Huerta, L. M., Cuevas-Covarrubias, S. A.

Publicada: 1 jul 2019
Resumen:


Filiaciones:
Messina-Baas, O. M.:
 Hosp Gen Mexico City, Oftalmol, Mexico City, DF, Mexico

Leon-Oviedo, C.:
 Hosp Gen Mexico City, Genet, Mexico City, DF, Mexico

Valdes-Miranda, J. M.:
 Hosp Gen Mexico City, Genet, Mexico City, DF, Mexico

Rivera-Vega, M. R.:
 Hosp Gen Mexico City, Genet, Mexico City, DF, Mexico

Vega-Gama, R.:
 Hosp Gen Mexico City, Genet, Mexico City, DF, Mexico

Xilotl-DeJesus, N.:
 Hosp Gen Mexico City, Genet, Mexico City, DF, Mexico

Martinez-Montoya, V.:
 Hosp Gen Mexico City, Genet, Mexico City, DF, Mexico

Tovar-Ayala, M. G.:
 Hosp Gen Mexico City, Genet, Mexico City, DF, Mexico

Gonzalez-Huerta, L. M.:
 Hosp Gen Mexico City, Genet, Mexico City, DF, Mexico

Cuevas-Covarrubias, S. A.:
 Univ Nacl Autonoma Mexico, Hosp Gen Mexico, Fac Med, Genet, Mexico City, DF, Mexico
ISSN: 10184813





EUROPEAN JOURNAL OF HUMAN GENETICS
Editorial
NATURE PUBLISHING GROUP, MACMILLAN BUILDING, 4 CRINAN ST, LONDON N1 9XW, ENGLAND, Reino Unido
Tipo de documento: Meeting Abstract
Volumen: 27 Número: 1
Páginas: 47-47
WOS Id: 000489313100098