Erratum to: A hypofunctional PAX1 mutation causes autosomal recessively inherited otofaciocervical syndrome

Pohl, Esther; Aykut, Ayca; Beleggia, Filippo; Karaca, Emin; Durmaz, Burak; Keupp, Katharina; Arslan, Esra; Palamar, Melis; Yigit, Gökhan; Özkinay, Ferda; Wollnik, Bernd

doi:10.1007/s00439-013-1341-0

Erratum to: A hypofunctional PAX1 mutation causes autosomal recessively inherited otofaciocervical syndrome

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Published: 25 July 2013

Volume 132, page 1321, (2013)
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Erratum to: A hypofunctional PAX1 mutation causes autosomal recessively inherited otofaciocervical syndrome

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Esther Pohl^1,2,3,
Ayca Aykut^1,4,
Filippo Beleggia^1,2,3,
Emin Karaca⁴,
Burak Durmaz⁴,
Katharina Keupp^1,2,3,
Esra Arslan⁴,
Melis Palamar⁵,
Gökhan Yigit^1,2,3,
Ferda Özkinay⁴ &
…
Bernd Wollnik^1,2,3

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The Original Article was published on 13 July 2013

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Erratum to: Hum Genet DOI 10.1007/s00439-013-1337-9

The name of author Melis Palamar Onay was published incorrectly. The correct name should read as Melis Palamar.

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Authors and Affiliations

Institute of Human Genetics, University Medical Faculty, University of Cologne, Kerpener Str. 34, 50931, Cologne, Germany
Esther Pohl, Ayca Aykut, Filippo Beleggia, Katharina Keupp, Gökhan Yigit & Bernd Wollnik
Center for Molecular Medicine Cologne (CMMC), University of Cologne, Cologne, Germany
Esther Pohl, Filippo Beleggia, Katharina Keupp, Gökhan Yigit & Bernd Wollnik
Cologne Excellence Cluster on Cellular Stress Responses in Aging-Associated Diseases (CECAD), University of Cologne, Cologne, Germany
Esther Pohl, Filippo Beleggia, Katharina Keupp, Gökhan Yigit & Bernd Wollnik
Department of Medical Genetics, Faculty of Medicine, Ege University, Izmir, Turkey
Ayca Aykut, Emin Karaca, Burak Durmaz, Esra Arslan & Ferda Özkinay
Department of Ophthalmology, Faculty of Medicine, Ege University, Izmir, Turkey
Melis Palamar

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Esther Pohl
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Ayca Aykut
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Filippo Beleggia
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Emin Karaca
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Burak Durmaz
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Katharina Keupp
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Esra Arslan
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Melis Palamar
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Gökhan Yigit
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Ferda Özkinay
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Bernd Wollnik
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Correspondence to Bernd Wollnik.

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The online version of the original article can be found under doi:10.1007/s00439-013-1337-9.

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Pohl, E., Aykut, A., Beleggia, F. et al. Erratum to: A hypofunctional PAX1 mutation causes autosomal recessively inherited otofaciocervical syndrome. Hum Genet 132, 1321 (2013). https://doi.org/10.1007/s00439-013-1341-0

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Published: 25 July 2013
Issue Date: November 2013
DOI: https://doi.org/10.1007/s00439-013-1341-0

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Erratum to: A hypofunctional PAX1 mutation causes autosomal recessively inherited otofaciocervical syndrome

Erratum to: Hum Genet DOI 10.1007/s00439-013-1337-9

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