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Correction to: Novel mutations in KMT2B offer pathophysiological insights on childhood-onset progressive dystonia (2019)

Hormos Salimi Dafsari, Rosanne Sprute, Gilbert Wunderlich, Hülya-Sevcan Daimagüler, Ezgi Karaca, Adriana Contreras, Kerstin Becker, Mira Schulze-Rhonhof, Karl Kiening, Tülay Karakulak, Manja Kloss, Annette Horn, Amande Pauls, Peter Nürnberg, Janine Al

Springer Nature

In: Journal of Human Genetics

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Publication Date: 2019

Print ISSN: 1434-5161

Electronic ISSN: 1435-232X

Topics: Biology , Medicine

Published by Springer Nature

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SOPH syndrome in three affected individuals showing similarities with progeroid cutis laxa conditions in early infancy (2019)

Björn Fischer-Zirnsak, Rainer Koenig, Franz Alisch, Nilay Güneş, Ingrid Hausser, Namrata Saha, Stefanie Beck-Woedl, Tobias B. Haack, Christian Thiel, Clemens Kamrath, Beyhan Tüysüz, Stephan Henning, Stefan Mundlos, Katrin Hoffmann, Denise Horn, Uwe K

Springer Nature

In: Journal of Human Genetics

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Publication Date: 2019

Print ISSN: 1434-5161

Electronic ISSN: 1435-232X

Topics: Biology , Medicine

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Correction to: Novel mutations in KMT2B offer pathophysiological insights on childhood-onset progressive dystonia (2019)

Dafsari, Hormos Salimi ; Sprute, Rosanne ; Wunderlich, Gilbert ; [et al.]

Springer Nature

In: Journal of Human Genetics. 2019; 64(10): 1051-1054. Published 2019 Aug 06. doi: 10.1038/s10038-019-0644-y.

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Publication Date: 2019-08-06

Print ISSN: 1434-5161

Electronic ISSN: 1435-232X

Topics: Biology , Medicine

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Novel mutations in KMT2B offer pathophysiological insights into childhood-onset progressive dystonia (2019)

Hormos Salimi Dafsari, Rosanne Sprute, Gilbert Wunderlich, Hülya-Sevcan Daimagüler, Ezgi Karaca, Adriana Contreras, Kerstin Becker, Mira Schulze-Rhonhof, Karl Kiening, Tülay Karakulak, Manja Kloss, Annette Horn, Amande Pauls, Peter Nürnberg, Janine Al

Springer Nature

In: Journal of Human Genetics

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Publication Date: 2019

Print ISSN: 1434-5161

Electronic ISSN: 1435-232X

Topics: Biology , Medicine

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SOPH syndrome in three affected individuals showing similarities with progeroid cutis laxa conditions in early infancy (2019)

Fischer-Zirnsak, Björn ; Koenig, Rainer ; Alisch, Franz ; [et al.]

Springer Nature

In: Journal of Human Genetics. 2019; 64(7): 609-616. Published 2019 Apr 24. doi: 10.1038/s10038-019-0602-8.

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Publication Date: 2019-04-24

Print ISSN: 1434-5161

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Topics: Biology , Medicine

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Novel mutations in KMT2B offer pathophysiological insights into childhood-onset progressive dystonia (2019)

Dafsari, Hormos Salimi ; Sprute, Rosanne ; Wunderlich, Gilbert ; [et al.]

Springer Nature

In: Journal of Human Genetics. 2019; 64(8): 803-813. Published 2019 Jun 05. doi: 10.1038/s10038-019-0625-1.

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Publication Date: 2019-06-05

Print ISSN: 1434-5161

Electronic ISSN: 1435-232X

Topics: Biology , Medicine

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