TY  - RPRT
TI  - Mutations in an unrecognized internal NPT2A PDZ motif disrupt phosphate transport causing congenital hypophosphatemia
AU  - Sneddon, W. B.
AU  - Friedman, P. A.
AU  - Mamonova, T.
PY  - 2023
DO  - 10.1101/2023.03.06.531332
UR  - https://www.biorxiv.org/content/10.1101/2023.03.06.531332v1
ID  - 10.1101/2023.03.06.531332
ER  -