5 years ago

Defective ATP breakdown activity related to an ENTPD1 gene mutation demonstrated using 31P NMR spectroscopy

Defective ATP breakdown activity related to an ENTPD1 gene mutation demonstrated using 31P NMR spectroscopy
Gal Sapir, Rachel Katz-Brull, J. Moshe Gomori, Or Kakhlon, Vardiella Meiner, Atara Nardi-Schreiber, Alexander Lossos, Jacob Sosna, Ayelet Gamliel
Quantification of the ENTPDase activity of human mononuclear cells by 31P NMR spectroscopy and the effect of a stop-codon mutation in the ENTPD1 gene.

Publisher URL: http://feeds.rsc.org/~r/rss/CC/~3/f1XzDORNcXg/C7CC00426E

DOI: 2017/CC/C7CC00426E

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