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

8 Citas (Scopus)

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 - Gong, Xin

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