Mutational Screening of FOXE3, GDF3, ATOH7, and ALDH1A3 in Congenital Ocular Malformations. Possible Contribution of the FOXE3 p.VAL201MET Variant to the Risk of Severe Eye Malformations
Por:
Garcia-Montalvo I.A., Pelcastre-Luna E., Nelson-Mora J., Buentello-Volante B., Miranda-Duarte A., Zenteno J.C.
Publicada:
1 sep 2014
Resumen:
[No abstract available]
Filiaciones:
Garcia-Montalvo I.A.:
Escuela de Nutricion, Universidad Regional Del Sureste (URSE), Oaxaca, Mexico
Pelcastre-Luna E.:
Department of Genetics-Research Unit, Institute of Ophthalmology Conde de Valenciana, Chimalpopoca 14, Col. Obrera, Mexico City, CP 06800, Mexico
Nelson-Mora J.:
Department of Genetics-Research Unit, Institute of Ophthalmology Conde de Valenciana, Chimalpopoca 14, Col. Obrera, Mexico City, CP 06800, Mexico
Buentello-Volante B.:
Department of Genetics-Research Unit, Institute of Ophthalmology Conde de Valenciana, Chimalpopoca 14, Col. Obrera, Mexico City, CP 06800, Mexico
Miranda-Duarte A.:
Department of Genetics, National Rehabilitation Institute, Mexico City, Mexico
Zenteno J.C.:
Univ Nacl Autonoma Mexico, Fac Med, Dept Biochem, Mexico City, DF, Mexico
Department of Genetics-Research Unit, Institute of Ophthalmology Conde de Valenciana, Chimalpopoca 14, Col. Obrera, Mexico City, CP 06800, Mexico
Department of Biochemistry, Faculty of Medicine, UNAM, Mexico City, Mexico
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