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

Fischer-Zirnsak, Bjoern; Koenig, Rainer; Alisch, Franz; Gunes, Nilay; Hausser, Ingrid; Saha, Namrata; Beck-Woedl, Stefanie; Haack, Tobias B.; Thiel, Christian; Kamrath, Clemens; Tuysuz, Beyhan; Henning, Stephan; Mundlos, Stefan; Hoffmann, Katrin; Horn, Denise; Kornak, Uwe

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

Autor(en):

Fischer-Zirnsak, Bjoern; Koenig, Rainer; Alisch, Franz; Gunes, Nilay; Hausser, Ingrid; Saha, Namrata; Beck-Woedl, Stefanie; Haack, Tobias B.; Thiel, Christian; Kamrath, Clemens; Tuysuz, Beyhan; Henning, Stephan; Mundlos, Stefan; Hoffmann, Katrin; Horn, Denise; Kornak, Uwe

Tübinger Autor(en):

Beck-Wödl, Stefanie
Haack, Tobias

Erschienen in:

Journal of Human Genetics (2019), Bd. 64, H. 7, S. 609-616

Verlagsangabe:

Nature Publishing Group

Sprache:

Englisch

Referenz zum Volltext:

http://dx.doi.org/10.1038/s10038-019-0602-8

ISSN:

1435-232X