Summary: brief report
The new england journal of medicine
n engl j med 348;17 www.nejm.org april 24, 20031664
A Mutation of PCDH15
among Ashkenazi Jews with the Type 1
Usher Syndrome
Tamar Ben-Yosef, Ph.D., Seth L. Ness, M.D., Ph.D., Anne C. Madeo, M.S.,
Adi Bar-Lev, M.S., Jessica H. Wolfman, Zubair M. Ahmed, Ph.D.,
Robert J. Desnick, M.D., Ph.D., Judith P. Willner, M.D., Karen B. Avraham, Ph.D.,
Harry Ostrer, M.D., Carole Oddoux, Ph.D., Andrew J. Griffith, M.D., Ph.D.,
and Thomas B. Friedman, Ph.D.
From the Laboratory of Molecular Genet-
ics, National Institute on Deafness and
Other Communication Disorders, National
Institutes of Health, Rockville, Md. (T.B.-Y.,
A.C.M., J.H.W., Z.M.A., A.J.G., T.B.F.); the
Department of Human Genetics, Mount
Sinai School of Medicine, New York (S.L.N.,
A.B.-L., R.J.D., J.P.W.); the Department of
Human Genetics and Molecular Medicine,

Source: Avraham, Karen - Department of Human Genetics and Molecular Medicine, Tel Aviv University

Collections: Biology and Medicine