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Fig. 1 | BMC Ophthalmology

Fig. 1

From: Genotype-phenotype associations in CRB1 bi-allelic patients: a novel mutation, a systematic review and meta-analysis

Fig. 1

The novel missense bi-allelic mutation c.2936G > A; p.(Gly979Asp) in crumbs cell polarity complex component 1 CRB1

A- Pedigree of the family with an index patient having a homozygous c.2936G > A; p.(Gly979Asp) in CRB1. B- Fundus auto-fluorescence images of the index patient (F23:V.1). Black symbol indicate affected member. Square and round symbols represent male and female individuals, respectively. The slash indicates deceased individuals. [M] defines mutated alleles. [ =] defines wild type alleles

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