Naegeli-Franceschetti-Jadassohn syndrome and dermatopathia pigmentosa reticularis: two allelic ectodermal dysplasias caused by dominant mutations in KRT14

Lugassy, J., Itin, P., Ishida-Yamamoto, A., Holland, K.R., Huson, S., Geiger, D., Hennies, Hans C., Indelman, M., Bercovich, D., Uitto, J., Bergman, R., McGrath, J.A., Richard, G. and Sprecher, E. (2006) Naegeli-Franceschetti-Jadassohn syndrome and dermatopathia pigmentosa reticularis: two allelic ectodermal dysplasias caused by dominant mutations in KRT14. American Journal of Human Genetics, 79 (4). pp. 724-730. ISSN 1537-6605

Information
Library
Statistics

[+][-]

Information

URI:

https://eprints.hud.ac.uk/id/eprint/28819

URI:

https://eprints.hud.ac.uk/id/eprint/28819

Title:

Naegeli-Franceschetti-Jadassohn syndrome and dermatopathia pigmentosa reticularis: two allelic ectodermal dysplasias caused by dominant mutations in KRT14

Creators:

Lugassy, J., Itin, P., Ishida-Yamamoto, A., Holland, K.R., Huson, S., Geiger, D., Hennies, Hans C., Indelman, M., Bercovich, D., Uitto, J., Bergman, R., McGrath, J.A., Richard, G. and Sprecher, E.

Identification Number:

https://doi.org/10.1086/507792

Official URL:

http://dx.doi.org/10.1086/507792

Date:

October 2006

Subjects:

Q Science > QH Natural history > QH301 Biology
Q Science > QH Natural history > QH426 Genetics

Schools:

School of Applied Sciences

Additional Information:

Unmapped bibliographic data: ST - Naegeli-Franceschetti-Jadassohn syndrome and dermatopathia pigmentosa reticularis: two allelic ectodermal dysplasias caused by dominant mutations in KRT14 [Field not mapped to EPrints] LB - 14 [Field not mapped to EPrints] RP - Not in File [Field not mapped to EPrints]

Uncontrolled Keywords:

analysis

Library

Item Type:

Article

Depositing User:

Hans Hennies

Date Deposited:

06 Jul 2016 13:52

Revision:

Last Modified:

28 Aug 2021 12:06

Statistics

CORE (COnnecting REpositories)

Tools