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Nadia Schoenmakers

Showing results (41-50 of 43) with videos related to

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The Journal of Clinical Investigation|November 19, 2010
Mutations in the selenocysteine insertion sequence-binding protein 2 gene lead to a multisystem selenoprotein deficiency disorder in humansErik Schoenmakers, Maura Agostini, Catherine Mitchell, et al.
Med (New York, N.Y.)|June 21, 2024
SMIM1 absence is associated with reduced energy expenditure and excess weightLuca Stefanucci, Camous Moslemi, Ana R Tomé, et al.
Nature Genetics|November 13, 2012
Loss-of-function mutations in IGSF1 cause an X-linked syndrome of central hypothyroidism and testicular enlargementYu Sun, Beata Bak, Nadia Schoenmakers, et al.
Pageof 5

Showing results (41-50 of 43) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 43 results.
The Journal of Clinical Investigation|November 19, 2010
Mutations in the selenocysteine insertion sequence-binding protein 2 gene lead to a multisystem selenoprotein deficiency disorder in humansErik Schoenmakers, Maura Agostini, Catherine Mitchell, et al.
Med (New York, N.Y.)|June 21, 2024
SMIM1 absence is associated with reduced energy expenditure and excess weightLuca Stefanucci, Camous Moslemi, Ana R Tomé, et al.
Nature Genetics|November 13, 2012
Loss-of-function mutations in IGSF1 cause an X-linked syndrome of central hypothyroidism and testicular enlargementYu Sun, Beata Bak, Nadia Schoenmakers, et al.
Pageof 5