| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
Announcement and Resource |
In the article "Novel fibroblast growth factor receptor 1 mutations in patients with congenital hypogonadotropic hypogonadism with and without anosmia" (J Clin Endocrinol Metab. 2006, 91:4006–4012), the mutation found in patient 7 is a 3-nt in-frame deletion c.1852_1854delAAG (p.K618del) and not c.1852–1853delAA (p.K618fsX654) as described in the article. The authors regret the error.
| ||||||||||||||||||||||||||||||||||||||||||||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| Endocrinology | Endocrine Reviews | J. Clin. End. & Metab. |
| Molecular Endocrinology | Recent Prog. Horm. Res. | All Endocrine Journals |