Exome sequencing reveals novel homozygous FOXE3 mutation in microphthalmos with staphylomatous malformation

Ujwala S. Saboo; Devi Penke; Avinash Mahindrakar; Madhu Uddaraju; Chandrasekhar Sankurathri; Xin Gong; Chao Xing; V. Vinod Mootha

doi:10.1080/13816810.2016.1217549

Exome sequencing reveals novel homozygous FOXE3 mutation in microphthalmos with staphylomatous malformation

Ujwala S. Saboo
, Devi Penke
, Avinash Mahindrakar
, Madhu Uddaraju
, Chandrasekhar Sankurathri
, Xin Gong
, Chao Xing
, V. Vinod Mootha

Producción científica: Letter › revisión exhaustiva

Idioma original	English (US)
Páginas (desde-hasta)	295-297
Número de páginas	3
Publicación	Ophthalmic Genetics
Volumen	38
N.º	3
DOI	https://doi.org/10.1080/13816810.2016.1217549
Estado	Published - may 4 2017
Publicado de forma externa	Sí

ASJC Scopus subject areas

Genetics(clinical)
Ophthalmology
Pediatrics, Perinatology, and Child Health

Acceder al documento

10.1080/13816810.2016.1217549

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AU - Sankurathri, Chandrasekhar

AU - Gong, Xin

AU - Xing, Chao

AU - Mootha, V. Vinod

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