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Home / CTGA Subject
CTGA Subject
Arab Genomic Studies

600974.5.1

Country
Morocco
HPO Terms
Hearing impairment
Sex
Female
Family History
Yes
Parental Consanguinity
No
Variants
NM_138691.2:c.1165C>T
NM_138691.2:c.1939T>C
References
Brownstein Z, Friedman LM, Shahin H, Oron-Karni V, Kol N, Rayyan AA, Parzefall T, Lev D, Shalev S, Frydman M, Davidov B, Shohat M, Rahile M, Lieberman S, Levy-Lahad E, Lee MK, Shomron N, King MC, Walsh T, Kanaan M, Avraham KB. Targeted genomic capture and massively parallel sequencing to identify genes for hereditary hearing loss in middle eastern families. Genome Biol. 2011; 12(9):R89.
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