Erratum: MPDU1 mutations underlie a novel human congenital disorder of glycosylation, designated type if (Journal of Clinical Investigation (2001) 108 (1687-1695))

Barbara Schenk; Timo Imbach; Christian G. Frank; Claudia E. Grubenmann; Gerald V. Raymond; Haggit Hurvitz; Isabelle Korn-Lubetzki; Shoshana Revel-Vik; Annick Raas-Rotschild; Anthony S. Luder; Jaak Jaeken; Eric G. Berger; Gert Matthijs; Thierry Hennet; Markus Aebi

doi:10.1172/JCI200316336C

Erratum: MPDU1 mutations underlie a novel human congenital disorder of glycosylation, designated type if (Journal of Clinical Investigation (2001) 108 (1687-1695))

Barbara Schenk, Timo Imbach, Christian G. Frank, Claudia E. Grubenmann, Gerald V. Raymond, Haggit Hurvitz, Isabelle Korn-Lubetzki, Shoshana Revel-Vik, Annick Raas-Rotschild, Anthony S. Luder, Jaak Jaeken, Eric G. Berger, Gert Matthijs, Thierry Hennet, Markus Aebi

Research output: Contribution to journal › Comment/debate › peer-review

Original language	English (US)
Pages (from-to)	925
Number of pages	1
Journal	Journal of Clinical Investigation
Volume	111
Issue number	6
DOIs	https://doi.org/10.1172/JCI200316336C
State	Published - Mar 2003
Externally published	Yes

Publisher link

10.1172/JCI200316336C

Find It

Find It at U of M Libraries

Cite this

Schenk, B., Imbach, T., Frank, C. G., Grubenmann, C. E., Raymond, G. V., Hurvitz, H., Korn-Lubetzki, I., Revel-Vik, S., Raas-Rotschild, A., Luder, A. S., Jaeken, J., Berger, E. G., Matthijs, G., Hennet, T., & Aebi, M. (2003). Erratum: MPDU1 mutations underlie a novel human congenital disorder of glycosylation, designated type if (Journal of Clinical Investigation (2001) 108 (1687-1695)). Journal of Clinical Investigation, 111(6), 925. https://doi.org/10.1172/JCI200316336C

Erratum: MPDU1 mutations underlie a novel human congenital disorder of glycosylation, designated type if (Journal of Clinical Investigation (2001) 108 (1687-1695)). / Schenk, Barbara; Imbach, Timo; Frank, Christian G. et al.
In: Journal of Clinical Investigation, Vol. 111, No. 6, 03.2003, p. 925.

Research output: Contribution to journal › Comment/debate › peer-review

Schenk, B, Imbach, T, Frank, CG, Grubenmann, CE, Raymond, GV, Hurvitz, H, Korn-Lubetzki, I, Revel-Vik, S, Raas-Rotschild, A, Luder, AS, Jaeken, J, Berger, EG, Matthijs, G, Hennet, T & Aebi, M 2003, 'Erratum: MPDU1 mutations underlie a novel human congenital disorder of glycosylation, designated type if (Journal of Clinical Investigation (2001) 108 (1687-1695))', Journal of Clinical Investigation, vol. 111, no. 6, pp. 925. https://doi.org/10.1172/JCI200316336C

@article{d7d601e765a14c3282b1f1d08e649cdb,

title = "Erratum: MPDU1 mutations underlie a novel human congenital disorder of glycosylation, designated type if (Journal of Clinical Investigation (2001) 108 (1687-1695))",

author = "Barbara Schenk and Timo Imbach and Frank, {Christian G.} and Grubenmann, {Claudia E.} and Raymond, {Gerald V.} and Haggit Hurvitz and Isabelle Korn-Lubetzki and Shoshana Revel-Vik and Annick Raas-Rotschild and Luder, {Anthony S.} and Jaak Jaeken and Berger, {Eric G.} and Gert Matthijs and Thierry Hennet and Markus Aebi",

year = "2003",

month = mar,

doi = "10.1172/JCI200316336C",

language = "English (US)",

volume = "111",

pages = "925",

journal = "Journal of Clinical Investigation",

issn = "0021-9738",

publisher = "American Society for Clinical Investigation",

number = "6",

}

TY - JOUR

T1 - Erratum

T2 - MPDU1 mutations underlie a novel human congenital disorder of glycosylation, designated type if (Journal of Clinical Investigation (2001) 108 (1687-1695))

AU - Schenk, Barbara

AU - Imbach, Timo

AU - Frank, Christian G.

AU - Grubenmann, Claudia E.

AU - Raymond, Gerald V.

AU - Hurvitz, Haggit

AU - Korn-Lubetzki, Isabelle

AU - Revel-Vik, Shoshana

AU - Raas-Rotschild, Annick

AU - Luder, Anthony S.

AU - Jaeken, Jaak

AU - Berger, Eric G.

AU - Matthijs, Gert

AU - Hennet, Thierry

AU - Aebi, Markus

PY - 2003/3

Y1 - 2003/3

UR - http://www.scopus.com/inward/record.url?scp=0042285651&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0042285651&partnerID=8YFLogxK

U2 - 10.1172/JCI200316336C

DO - 10.1172/JCI200316336C

M3 - Comment/debate

AN - SCOPUS:0042285651

SN - 0021-9738

VL - 111

SP - 925

JO - Journal of Clinical Investigation

JF - Journal of Clinical Investigation

IS - 6

ER -

Erratum: MPDU1 mutations underlie a novel human congenital disorder of glycosylation, designated type if (Journal of Clinical Investigation (2001) 108 (1687-1695))

Publisher link

Find It

Other files and links

Cite this