Fatal outcome due to deficiency of subunit 6 of the conserved oligomeric Golgi complex leading to a new type of congenital disorders of glycosylation.

J. Lubbehusen; C. Thiel; N. Rind; D. Ungar; H.C.M.T. Prinsen; T.J. de Koning; P.M. van Hasselt; C. Korner

Fatal outcome due to deficiency of subunit 6 of the conserved oligomeric Golgi complex leading to a new type of congenital disorders of glycosylation.

Translated title of the contribution: Fatal outcome due to deficiency of subunit 6 of the conserved oligomeric Golgi complex leading to a new type of congenital disorders of glycosylation.

J. Lubbehusen
, C. Thiel
, N. Rind
, D. Ungar
, H.C.M.T. Prinsen
, T.J. de Koning
, P.M. van Hasselt
, C. Korner

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

Translated title of the contribution	Fatal outcome due to deficiency of subunit 6 of the conserved oligomeric Golgi complex leading to a new type of congenital disorders of glycosylation.
Original language	Undefined/Unknown
Pages (from-to)	3623-3633
Number of pages	11
Journal	Human Molecular Genetics
Volume	19
Issue number	18
Publication status	Published - 2010

Cite this

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title = "Fatal outcome due to deficiency of subunit 6 of the conserved oligomeric Golgi complex leading to a new type of congenital disorders of glycosylation.",

author = "J. Lubbehusen and C. Thiel and N. Rind and D. Ungar and H.C.M.T. Prinsen and \{de Koning\}, T.J. and \{van Hasselt\}, P.M. and C. Korner",

year = "2010",

language = "Undefined/Unknown",

volume = "19",

pages = "3623--3633",

journal = "Human Molecular Genetics",

issn = "0964-6906",

publisher = "Oxford University Press",

number = "18",

}

TY - JOUR

T1 - Fatal outcome due to deficiency of subunit 6 of the conserved oligomeric Golgi complex leading to a new type of congenital disorders of glycosylation.

AU - Lubbehusen, J.

AU - Thiel, C.

AU - Rind, N.

AU - Ungar, D.

AU - Prinsen, H.C.M.T.

AU - de Koning, T.J.

AU - van Hasselt, P.M.

AU - Korner, C.

PY - 2010

Y1 - 2010

M3 - Article

SN - 0964-6906

VL - 19

SP - 3623

EP - 3633

JO - Human Molecular Genetics

JF - Human Molecular Genetics

IS - 18

ER -