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Loss of function variants in human PNPLA8 encoding calcium-independent phospholipase A2 γ recapitulate the mitochondriopathy of the homologous null mouse. [electronic resource] by
- Saunders, Carol J
- Moon, Sung Ho
- Liu, Xinping
- Thiffault, Isabelle
- Coffman, Keith
- LePichon, Jean-Baptiste
- Taboada, Eugenio
- Smith, Laurie D
- Farrow, Emily G
- Miller, Neil
- Gibson, Margaret
- Patterson, Melanie
- Kingsmore, Stephen F
- Gross, Richard W
Producer: 20151125
In:
Human mutation vol. 36
Availability: No items available.
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