A Founder Mutation in MYO7A Underlies a Significant Proportion of Usher Syndrome in Indigenous South Africans: Implications for the African Diaspora.

Roberts, Lisa; George, Siddiqah; Greenberg, Jacquie; Ramesar, Raj S

Roberts, Lisa; George, Siddiqah; Greenberg, Jacquie; Ramesar, Raj S.

Invest Ophthalmol Vis Sci ; 56(11): 6671-8, 2015 Oct.

Article in En | MEDLINE | ID: mdl-26469752

Subject(s)

Black People/genetics; Human Migration; Myosins/genetics; Sequence Deletion/genetics; Usher Syndromes/genetics; Alleles; Ethnicity/genetics; Female; Gene Frequency/genetics; Haplotypes/genetics; Homozygote; Humans; Male; Myosin VIIa; Pedigree; Polymorphism, Single Nucleotide/genetics; South Africa/epidemiology

Fulltext

XML

PubMed Links

Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Myosins / Sequence Deletion / Black People / Usher Syndromes / Human Migration Type of study: Prognostic_studies Limits: Female / Humans / Male Country/Region as subject: Africa Language: En Journal: Invest Ophthalmol Vis Sci Year: 2015 Type: Article

Fulltext

XML

PubMed Links

Search on Google