A novel loss-of-function mutation in the proton-coupled folate transporter from a patient with hereditary folate malabsorption reveals that Arg 113 is crucial for function

I. Lasry, B. Berman, R. Straussberg, Y. Sofer, H. Bessler, M. Sharkia, F. Glaser, G. Jansen, S. Drori, Y.G. Assaraf

Research output: Contribution to journal › Article › Academic › peer-review

Original languageUndefined/Unknown
Pages (from-to)2055-2061
JournalBlood
Volume112
Issue number5
DOIs
Publication statusPublished - 2008

Cite this

Lasry, I. ; Berman, B. ; Straussberg, R. ; Sofer, Y. ; Bessler, H. ; Sharkia, M. ; Glaser, F. ; Jansen, G. ; Drori, S. ; Assaraf, Y.G. / A novel loss-of-function mutation in the proton-coupled folate transporter from a patient with hereditary folate malabsorption reveals that Arg 113 is crucial for function. In: Blood. 2008 ; Vol. 112, No. 5. pp. 2055-2061.
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title = "A novel loss-of-function mutation in the proton-coupled folate transporter from a patient with hereditary folate malabsorption reveals that Arg 113 is crucial for function",
author = "I. Lasry and B. Berman and R. Straussberg and Y. Sofer and H. Bessler and M. Sharkia and F. Glaser and G. Jansen and S. Drori and Y.G. Assaraf",
year = "2008",
doi = "10.1182/blood-2008-04-150276",
language = "Undefined/Unknown",
volume = "112",
pages = "2055--2061",
journal = "Blood",
issn = "0006-4971",
publisher = "American Society of Hematology",
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Lasry, I, Berman, B, Straussberg, R, Sofer, Y, Bessler, H, Sharkia, M, Glaser, F, Jansen, G, Drori, S & Assaraf, YG 2008, 'A novel loss-of-function mutation in the proton-coupled folate transporter from a patient with hereditary folate malabsorption reveals that Arg 113 is crucial for function' Blood, vol. 112, no. 5, pp. 2055-2061. https://doi.org/10.1182/blood-2008-04-150276

A novel loss-of-function mutation in the proton-coupled folate transporter from a patient with hereditary folate malabsorption reveals that Arg 113 is crucial for function. / Lasry, I.; Berman, B.; Straussberg, R.; Sofer, Y.; Bessler, H.; Sharkia, M.; Glaser, F.; Jansen, G.; Drori, S.; Assaraf, Y.G.

In: Blood, Vol. 112, No. 5, 2008, p. 2055-2061.

Research output: Contribution to journal › Article › Academic › peer-review

TY - JOUR

T1 - A novel loss-of-function mutation in the proton-coupled folate transporter from a patient with hereditary folate malabsorption reveals that Arg 113 is crucial for function

AU - Lasry, I.

AU - Berman, B.

AU - Straussberg, R.

AU - Sofer, Y.

AU - Bessler, H.

AU - Sharkia, M.

AU - Glaser, F.

AU - Jansen, G.

AU - Drori, S.

AU - Assaraf, Y.G.

PY - 2008

Y1 - 2008

U2 - 10.1182/blood-2008-04-150276

DO - 10.1182/blood-2008-04-150276

M3 - Article

VL - 112

SP - 2055

EP - 2061

JO - Blood

JF - Blood

SN - 0006-4971

IS - 5

ER -

Lasry I, Berman B, Straussberg R, Sofer Y, Bessler H, Sharkia M et al. A novel loss-of-function mutation in the proton-coupled folate transporter from a patient with hereditary folate malabsorption reveals that Arg 113 is crucial for function. Blood. 2008;112(5):2055-2061. https://doi.org/10.1182/blood-2008-04-150276

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