Correction to: A zebrafish model of foxe3 deficiency demonstrates lens and eye defects with dysregulation of key genes involved in cataract formation in humans (Human Genetics, (2018), 137, 4, (315-328), 10.1007/s00439-018-1884-1)

M. Krall; S. Htun; D. Anand; D. Hart; S. A. Lachke; A. M. Slavotinek

doi:10.1007/s00439-018-1890-3

Correction to: A zebrafish model of foxe3 deficiency demonstrates lens and eye defects with dysregulation of key genes involved in cataract formation in humans (Human Genetics, (2018), 137, 4, (315-328), 10.1007/s00439-018-1884-1)

M. Krall
, S. Htun
, D. Anand
, D. Hart
, S. A. Lachke
, A. M. Slavotinek

University of California at San Francisco
University of Delaware

Research output: Contribution to journal › Comment/debate

Abstract

The authors noticed that Fig. 5A and B aspect ratios appeared sub-optimal in the online published version. This has now been changed.

Original language	English
Pages (from-to)	427-428
Number of pages	2
Journal	Human Genetics
Volume	137
Issue number	5
DOIs	https://doi.org/10.1007/s00439-018-1890-3
State	Published - 1 May 2018
Externally published	Yes

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Krall, M., Htun, S., Anand, D., Hart, D., Lachke, S. A., & Slavotinek, A. M. (2018). Correction to: A zebrafish model of foxe3 deficiency demonstrates lens and eye defects with dysregulation of key genes involved in cataract formation in humans (Human Genetics, (2018), 137, 4, (315-328), 10.1007/s00439-018-1884-1). Human Genetics, 137(5), 427-428. https://doi.org/10.1007/s00439-018-1890-3

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title = "Correction to: A zebrafish model of foxe3 deficiency demonstrates lens and eye defects with dysregulation of key genes involved in cataract formation in humans (Human Genetics, (2018), 137, 4, (315-328), 10.1007/s00439-018-1884-1)",

abstract = "The authors noticed that Fig. 5A and B aspect ratios appeared sub-optimal in the online published version. This has now been changed.",

author = "M. Krall and S. Htun and D. Anand and D. Hart and Lachke, \{S. A.\} and Slavotinek, \{A. M.\}",

note = "Publisher Copyright: {\textcopyright} 2018, Springer-Verlag GmbH Germany, part of Springer Nature.",

year = "2018",

month = may,

day = "1",

doi = "10.1007/s00439-018-1890-3",

language = "English",

volume = "137",

pages = "427--428",

journal = "Human Genetics",

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number = "5",

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Krall, M, Htun, S, Anand, D, Hart, D, Lachke, SA & Slavotinek, AM 2018, 'Correction to: A zebrafish model of foxe3 deficiency demonstrates lens and eye defects with dysregulation of key genes involved in cataract formation in humans (Human Genetics, (2018), 137, 4, (315-328), 10.1007/s00439-018-1884-1)', Human Genetics, vol. 137, no. 5, pp. 427-428. https://doi.org/10.1007/s00439-018-1890-3

Correction to: A zebrafish model of foxe3 deficiency demonstrates lens and eye defects with dysregulation of key genes involved in cataract formation in humans (Human Genetics, (2018), 137, 4, (315-328), 10.1007/s00439-018-1884-1). / Krall, M.; Htun, S.; Anand, D. et al.
In: Human Genetics, Vol. 137, No. 5, 01.05.2018, p. 427-428.

Research output: Contribution to journal › Comment/debate

TY - JOUR

T1 - Correction to

T2 - A zebrafish model of foxe3 deficiency demonstrates lens and eye defects with dysregulation of key genes involved in cataract formation in humans (Human Genetics, (2018), 137, 4, (315-328), 10.1007/s00439-018-1884-1)

AU - Krall, M.

AU - Htun, S.

AU - Anand, D.

AU - Hart, D.

AU - Lachke, S. A.

AU - Slavotinek, A. M.

PY - 2018/5/1

Y1 - 2018/5/1

N2 - The authors noticed that Fig. 5A and B aspect ratios appeared sub-optimal in the online published version. This has now been changed.

AB - The authors noticed that Fig. 5A and B aspect ratios appeared sub-optimal in the online published version. This has now been changed.

UR - https://www.scopus.com/pages/publications/85046752086

U2 - 10.1007/s00439-018-1890-3

DO - 10.1007/s00439-018-1890-3

M3 - Comment/debate

C2 - 29752539

AN - SCOPUS:85046752086

SN - 0340-6717

VL - 137

SP - 427

EP - 428

JO - Human Genetics

JF - Human Genetics

IS - 5

ER -

Correction to: A zebrafish model of foxe3 deficiency demonstrates lens and eye defects with dysregulation of key genes involved in cataract formation in humans (Human Genetics, (2018), 137, 4, (315-328), 10.1007/s00439-018-1884-1)

Abstract

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