A novel CISD2 mutation associated with a classical Wolfram syndrome phenotype alters Ca2+ homeostasis and ER-mitochondria interactions
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P. Yu-Wai-Man | A. Chaussenot | S. Bannwarth | F. Burté | M. Catala | V. Serre | S. Lacas‐Gervais | C. Rouzier | K. Fragaki | C. Delorme | D. Moore | V. Paquis-Flucklinger | S. Ait-El-Mkadem