A new Fgf10 mutation in the mouse leads to atrophy of the harderian gland and slit-eye phenotype in heterozygotes: A novel model for dry-eye disease?
Dokumenttyp:
Zeitschriftenaufsatz
Autor(en):
Puk, O. ; Esposito, I. ; Söker, T. ; Löster, J. ; Budde, B. ; Nürnberg, P. ; Michel-Soewarto, D. ; Fuchs, H. ; Wolf, E. ; Hrabé de Angelis, M. ; Graw, J.
Stichworte:
Genetics and Epidemiology ; Enabling and Novel Technologies