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

doi: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

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

Rheumatology

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

Original language	Undefined/Unknown
Pages (from-to)	2055-2061
Journal	Blood
Volume	112
Issue number	5
DOIs	https://doi.org/10.1182/blood-2008-04-150276
Publication status	Published - 2008

Access to Document

10.1182/blood-2008-04-150276

Cite this

Lasry, I., Berman, B., Straussberg, R., Sofer, Y., Bessler, H., Sharkia, M., ... Assaraf, Y. G. (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, 112(5), 2055-2061. https://doi.org/10.1182/blood-2008-04-150276

@article{7bc77365e714452db74ee556a701a704,

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",

number = "5",

}

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

C2 - 18559978

VL - 112

SP - 2055

EP - 2061

JO - Blood

JF - Blood

SN - 0006-4971

IS - 5

ER -