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Frontiers in Physiology
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June 25, 2019
Dysfunctional LAT2 Amino Acid Transporter Is Associated With Cataract in Mouse and Humans
Emilia Boiadjieva Knöpfel, Clara Vilches, Simone M R Camargo, et al.
Nature Genetics
|
August 3, 2004
Mutations in SLC6A19, encoding B0AT1, cause Hartnup disorder
Robert Kleta, Elisa Romeo, Zorica Ristic, et al.
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Search research articles
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Showing results (31-40 of 32) with videos related to
Sort By:
Page
of 4
You have reached the last page of results.
This site can display upto 32 results.
Frontiers in Physiology
|
June 25, 2019
Dysfunctional LAT2 Amino Acid Transporter Is Associated With Cataract in Mouse and Humans
Emilia Boiadjieva Knöpfel, Clara Vilches, Simone M R Camargo, et al.
Nature Genetics
|
August 3, 2004
Mutations in SLC6A19, encoding B0AT1, cause Hartnup disorder
Robert Kleta, Elisa Romeo, Zorica Ristic, et al.
Page
of 4