Predominance and clustering of splice-site variants in Koreans with IMPG2-associated retinopathy: implications for haploinsufficiency and loss of function as disease mechanisms.

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Predominance and clustering of splice-site variants in Koreans with IMPG2-associated retinopathy: implications for haploinsufficiency and loss of function as disease mechanisms. | بیمارستان چشم پزشکی نور البرز

Predominance and clustering of splice-site variants in Koreans with IMPG2-associated retinopathy: implications for haploinsufficiency and loss of function as disease mechanisms.

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