Preliminary report on screening IGSF3 gene mutation in families with congenital absence of lacrimal puncta and canaliculi.

Wang, Fei; Tao, Hai; Han, Cui; Bai, Fang; Wang, Peng; Zhou, Xi-Bin; Wang, Li-Hua; Liu, Chuan

Wang, Fei; Tao, Hai; Han, Cui; Bai, Fang; Wang, Peng; Zhou, Xi-Bin; Wang, Li-Hua; Liu, Chuan.

Afiliação

Wang F; Lacrimal Center of Ophthalmology, the Third Medical Center of Chinese PLA General Hospital, Beijing 100039, China.
Tao H; Lacrimal Center of Ophthalmology, the Third Medical Center of Chinese PLA General Hospital, Beijing 100039, China.
Han C; Lacrimal Center of Ophthalmology, the Third Medical Center of Chinese PLA General Hospital, Beijing 100039, China.
Bai F; Lacrimal Center of Ophthalmology, the Third Medical Center of Chinese PLA General Hospital, Beijing 100039, China.
Wang P; Lacrimal Center of Ophthalmology, the Third Medical Center of Chinese PLA General Hospital, Beijing 100039, China.
Zhou XB; Lacrimal Center of Ophthalmology, the Third Medical Center of Chinese PLA General Hospital, Beijing 100039, China.
Wang LH; Lacrimal Center of Ophthalmology, the Third Medical Center of Chinese PLA General Hospital, Beijing 100039, China.
Liu C; Lacrimal Center of Ophthalmology, the Third Medical Center of Chinese PLA General Hospital, Beijing 100039, China.

Int J Ophthalmol ; 13(9): 1351-1355, 2020.

Article em En | MEDLINE | ID: mdl-32953570

Palavras-chave

DNA sequencing; IGSF3 mutation; congenital absence; lacrimal canaliculi; lacrimal puncta

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies / Screening_studies Idioma: En Revista: Int J Ophthalmol Ano de publicação: 2020 Tipo de documento: Article

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