The anhidrotic ectodermal dysplasia gene (EDA) undergoes alternative splicing and encodes ectodysplasin-A with deletion mutations in collagenous repeats

Author： Hartung A.J.  

Publisher： Oxford University Press

E-ISSN： 0964-6906|7|11|1661-1669

ISSN： 1460-2083

Source： Human Molecular Genetics, Vol.7, Iss.11, 1998-11, pp. : 1661-1669

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Related content

Anhidrotic Ectodermal Dysplasia (EDA) Protein Expressed in MCF-7 Cells Associates with Cell Membrane and Induces Rounding

By Ezer Sini   Schlessinger David   Srivastava Anand   Kere Juha  

Human Molecular Genetics, Vol. 6, Iss. 9, 1997-01 ,pp. : 1581-1587

Oxford University Press

Access to resources Recommend Favorite

Cloning of Tabby , the Murine Homolog of the Human EDA Gene: Evidence for a Membrane-Associated Protein with a Short Collagenous Domain

By Ferguson Betsy M.   Brockdorff Neil   Formstone Emma   Ngyuen Tung   Kronmiller Jan E.   Zonana Jonathan  

Human Molecular Genetics, Vol. 6, Iss. 9, 1997-01 ,pp. : 1589-1594

Oxford University Press

Access to resources Recommend Favorite

Connexin30 mutations responsible for hidrotic ectodermal dysplasia cause abnormal hemichannel activity

By Essenfelder Guilherme Munhoz  

Human Molecular Genetics, Vol. 13, Iss. 16, 2004-08 ,pp. : 1703-1714

Oxford University Press

Access to resources Recommend Favorite

A Plakophilin-1 Gene Mutation in an Egyptian Family with Ectodermal Dysplasia-Skin Fragility Syndrome

By  

Molecular Syndromology, Vol. 5, Iss. 6, 2014-11 ,pp. : 304-306

Karger

Access to resources Recommend Favorite

Testicular dysgenesis/regression without campomelic dysplasia in patients carrying missense mutations and upstream deletion of SOX9

By  

Molecular Genetics & Genomic Medicine, Vol. 3, Iss. 6, 2015-11 ,pp. : 550-557

John Wiley & Sons Inc

Access to resources Recommend Favorite