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Author/Creator Moya, Graciela

2. Clinical features and possible founder mutation of the 8bp duplication mutation in the SLC4A11 gene causing corneal dystrophy and perceptive deafness in three South American families. (4th March 2019)

Authors:
Romero, Pablo T.; Donoso, Rodrigo; López, Pamela; Miranda, Ana; Rodríguez, Leandro; Chrzanowsky, Dominique; Asenjo, Maria S.; Burgos, Gonzalo; Villegas, Pablo; Desir, Julie; Moya, Graciela; Herrera, Luisa M.
Journal:
Ophthalmic genetics
Issue:
Volume 40:Number 2(2019)
Page Start:
91
Record Type:
Journal Article
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