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Association of common genetic variation in the insulin/IGF1 signaling pathway with human longevity. [electronic resource] by
- Pawlikowska, Ludmila
- Hu, Donglei
- Huntsman, Scott
- Sung, Andrew
- Chu, Catherine
- Chen, Justin
- Joyner, Alexander H
- Schork, Nicholas J
- Hsueh, Wen-Chi
- Reiner, Alexander P
- Psaty, Bruce M
- Atzmon, Gil
- Barzilai, Nir
- Cummings, Steven R
- Browner, Warren S
- Kwok, Pui-Yan
- Ziv, Elad
Producer: 20091026
In:
Aging cell vol. 8
Availability: No items available.
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Pathogenic Bi-allelic Mutations in NDUFAF8 Cause Leigh Syndrome with an Isolated Complex I Deficiency. [electronic resource] by
- Alston, Charlotte L
- Veling, Mike T
- Heidler, Juliana
- Taylor, Lucie S
- Alaimo, Joseph T
- Sung, Andrew Y
- He, Langping
- Hopton, Sila
- Broomfield, Alexander
- Pavaine, Julija
- Diaz, Jullianne
- Leon, Eyby
- Wolf, Philipp
- McFarland, Robert
- Prokisch, Holger
- Wortmann, Saskia B
- Bonnen, Penelope E
- Wittig, Ilka
- Pagliarini, David J
- Taylor, Robert W
Producer: 20200417
In:
American journal of human genetics vol. 106
Availability: No items available.
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