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Ian C Scott

Showing results (121-130 of 124) with videos related to

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Nature|September 3, 2025
Genetic suppression features ABHD18 as a Barth syndrome therapeutic targetSanna N Masud, Anchal Srivastava, Patricia Mero, et al.
American Journal of Human Genetics|February 12, 2026
A cardiovascular, craniofacial, and neurodevelopmental disorder caused by loss-of-function variants in the eIF3 complex component genes EIF3A and EIF3BEsra Erkut, Cherith Somerville, Marci L B Schwartz, et al.
American Journal of Human Genetics|October 1, 2025
A cardiovascular, craniofacial, and neurodevelopmental disorder caused by loss-of-function variants in the eIF3 complex component genes EIF3A and EIF3BEsra Erkut, Cherith Somerville, Marci L B Schwartz, et al.
Nature Genetics|November 5, 2022
Multi-ancestry genome-wide association analyses identify novel genetic mechanisms in rheumatoid arthritisKazuyoshi Ishigaki, Saori Sakaue, Chikashi Terao, et al.
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Showing results (121-130 of 124) with videos related to

Sort By:
Pageof 13
You have reached the last page of results.This site can display upto 124 results.
Nature|September 3, 2025
Genetic suppression features ABHD18 as a Barth syndrome therapeutic targetSanna N Masud, Anchal Srivastava, Patricia Mero, et al.
American Journal of Human Genetics|February 12, 2026
A cardiovascular, craniofacial, and neurodevelopmental disorder caused by loss-of-function variants in the eIF3 complex component genes EIF3A and EIF3BEsra Erkut, Cherith Somerville, Marci L B Schwartz, et al.
American Journal of Human Genetics|October 1, 2025
A cardiovascular, craniofacial, and neurodevelopmental disorder caused by loss-of-function variants in the eIF3 complex component genes EIF3A and EIF3BEsra Erkut, Cherith Somerville, Marci L B Schwartz, et al.
Nature Genetics|November 5, 2022
Multi-ancestry genome-wide association analyses identify novel genetic mechanisms in rheumatoid arthritisKazuyoshi Ishigaki, Saori Sakaue, Chikashi Terao, et al.
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