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

Crossref DOI link: https://doi.org/10.1039/C7CC00426E

Published Online: 2017

Update policy: https://doi.org/10.1039/rsc_crossmark_policy

Authors

Nardi-Schreiber, Atara https://orcid.org/0000-0001-6321-1233
Sapir, Gal https://orcid.org/0000-0001-6267-5933
Gamliel, Ayelet

Kakhlon, Or

Sosna, Jacob

Gomori, J. Moshe

Meiner, Vardiella

Lossos, Alexander

Katz-Brull, Rachel https://orcid.org/0000-0003-4850-1616
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RELATED DATA

: Supplementary Information

IDENTIFIERS

: Atara Nardi-Schreiber (ORCID)

: Gal Sapir (ORCID)

: Rachel Katz-Brull (ORCID)

COPYRIGHT AND LICENSING

: The Royal Society of Chemistry has an exclusive publication licence for this journal

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PUBLICATION HISTORY

: Received 17 January 2017; Accepted 21 July 2017; Advance Article published 31 July 2017; Version of Record published 10 August 2017