Critical involvement of ZEB2 in collagen fibrillogenesis: the molecular similarity between Mowat-Wilson syndrome and Ehlers-Danlos syndrome-Reference-Cited by-同舟云学术

Critical involvement of ZEB2 in collagen fibrillogenesis: the molecular similarity between Mowat-Wilson syndrome and Ehlers-Danlos syndrome

Published:2017-04-19 Issue:1 Volume:7 Page:
ISSN:2045-2322
Container-title:Scientific Reports
language:en
Short-container-title:Sci Rep

Author:

Teraishi Mika,Takaishi Mikiro,Nakajima Kimiko,Ikeda Mitsunori,Higashi Yujiro,Shimoda Shinji,Asada Yoshinobu,Hijikata Atsushi,Ohara Osamu,Hiraki Yoko,Mizuno Seiji,Fukada Toshiyuki,Furukawa Takahisa,Wakamatsu Nobuaki,Sano Shigetoshi

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Link

http://www.nature.com/articles/srep46565.pdf

Reference34 articles.

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2. Mowat, D. Mowat-Wilson syndrome. Management of genetic syndromes (ed. Cassidy, S. B. & Allanson, J. E. ) 517–527 (Wiley-Blackwell, 2010).

3. Yamada, Y. et al. The spectrum of ZEB2 mutations causing the Mowat-Wilson syndrome in Japanese populations. Am. J. Med. Genet. 164A, 1899–1908 (2014).

4. Adam, M. P. et al. Mowat-Wilson Syndrome in GeneReviews[Internet] https://www.ncbi.nlm.nih.gov/books/NBK1412/ (2013).

5. Mowat, D. R. et al. Hirschsprung disease, microcephaly, mental retardation, and characteristic facial features: delineation of a new syndrome and identification of a locus at chromosome 2q22-q23. J. Med. Genet. 35, 617–623 (1998).

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