Erratum: A common mutation in the COG7 gene with a consistent phenotype including microcephaly, adducted thumbs, growth retardation, VSD and episodes of hyperthermia (European Journal of Human Genetics (2007) vol. 15 (638-645) 10.1038/sj.ejhg.5201813)

Eva Morava; Renate Zeevaert; Eckhard Korsch; Karin Huijben; Suzan Wopereis; Gert Matthijs; Kathelijn Keymolen; Dirk J. Lefeber; Linda De Meirleir; Ron A. Wevers

doi:10.1038/sj.ejhg.5201863

Erratum: A common mutation in the COG7 gene with a consistent phenotype including microcephaly, adducted thumbs, growth retardation, VSD and episodes of hyperthermia (European Journal of Human Genetics (2007) vol. 15 (638-645) 10.1038/sj.ejhg.5201813)

Eva Morava, Renate Zeevaert, Eckhard Korsch, Karin Huijben, Suzan Wopereis, Gert Matthijs, Kathelijn Keymolen, Dirk J. Lefeber, Linda De Meirleir, Ron A. Wevers

Genetics and Genomic Sciences

Research output: Contribution to journal › Comment/debate

Original language	English
Pages (from-to)	819
Number of pages	1
Journal	European Journal of Human Genetics
Volume	15
Issue number	7
DOIs	https://doi.org/10.1038/sj.ejhg.5201863
State	Published - Jul 2007

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10.1038/sj.ejhg.5201863

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Morava, E., Zeevaert, R., Korsch, E., Huijben, K., Wopereis, S., Matthijs, G., Keymolen, K., Lefeber, D. J., De Meirleir, L., & Wevers, R. A. (2007). Erratum: A common mutation in the COG7 gene with a consistent phenotype including microcephaly, adducted thumbs, growth retardation, VSD and episodes of hyperthermia (European Journal of Human Genetics (2007) vol. 15 (638-645) 10.1038/sj.ejhg.5201813). European Journal of Human Genetics, 15(7), 819. https://doi.org/10.1038/sj.ejhg.5201863

Morava, Eva ; Zeevaert, Renate ; Korsch, Eckhard et al. / Erratum : A common mutation in the COG7 gene with a consistent phenotype including microcephaly, adducted thumbs, growth retardation, VSD and episodes of hyperthermia (European Journal of Human Genetics (2007) vol. 15 (638-645) 10.1038/sj.ejhg.5201813). In: European Journal of Human Genetics. 2007 ; Vol. 15, No. 7. pp. 819.

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title = "Erratum: A common mutation in the COG7 gene with a consistent phenotype including microcephaly, adducted thumbs, growth retardation, VSD and episodes of hyperthermia (European Journal of Human Genetics (2007) vol. 15 (638-645) 10.1038/sj.ejhg.5201813)",

author = "Eva Morava and Renate Zeevaert and Eckhard Korsch and Karin Huijben and Suzan Wopereis and Gert Matthijs and Kathelijn Keymolen and Lefeber, {Dirk J.} and {De Meirleir}, Linda and Wevers, {Ron A.}",

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Morava, E, Zeevaert, R, Korsch, E, Huijben, K, Wopereis, S, Matthijs, G, Keymolen, K, Lefeber, DJ, De Meirleir, L & Wevers, RA 2007, 'Erratum: A common mutation in the COG7 gene with a consistent phenotype including microcephaly, adducted thumbs, growth retardation, VSD and episodes of hyperthermia (European Journal of Human Genetics (2007) vol. 15 (638-645) 10.1038/sj.ejhg.5201813)', European Journal of Human Genetics, vol. 15, no. 7, pp. 819. https://doi.org/10.1038/sj.ejhg.5201863

Erratum: A common mutation in the COG7 gene with a consistent phenotype including microcephaly, adducted thumbs, growth retardation, VSD and episodes of hyperthermia (European Journal of Human Genetics (2007) vol. 15 (638-645) 10.1038/sj.ejhg.5201813). / Morava, Eva; Zeevaert, Renate; Korsch, Eckhard et al.
In: European Journal of Human Genetics, Vol. 15, No. 7, 07.2007, p. 819.

Research output: Contribution to journal › Comment/debate

TY - JOUR

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AU - Morava, Eva

AU - Zeevaert, Renate

AU - Korsch, Eckhard

AU - Huijben, Karin

AU - Wopereis, Suzan

AU - Matthijs, Gert

AU - Keymolen, Kathelijn

AU - Lefeber, Dirk J.

AU - De Meirleir, Linda

AU - Wevers, Ron A.

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DO - 10.1038/sj.ejhg.5201863

M3 - Comment/debate

AN - SCOPUS:34250698883

SN - 1018-4813

VL - 15

SP - 819

JO - European Journal of Human Genetics

JF - European Journal of Human Genetics

IS - 7

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Morava E, Zeevaert R, Korsch E, Huijben K, Wopereis S, Matthijs G et al. Erratum: A common mutation in the COG7 gene with a consistent phenotype including microcephaly, adducted thumbs, growth retardation, VSD and episodes of hyperthermia (European Journal of Human Genetics (2007) vol. 15 (638-645) 10.1038/sj.ejhg.5201813). European Journal of Human Genetics. 2007 Jul;15(7):819. doi: 10.1038/sj.ejhg.5201863