Molecular genetics of familial central diabetes insipidus

Editorial

W L Miller. J Clin Endocrinol Metab. 1993 Sep.

. 1993 Sep;77(3):592-5.

doi: 10.1210/jcem.77.3.8370680.

No abstract available

Comment on

Glu-47, which forms a salt bridge between neurophysin-II and arginine vasopressin, is deleted in patients with familial central diabetes insipidus.
Yuasa H, Ito M, Nagasaki H, Oiso Y, Miyamoto S, Sasaki N, Saito H. Yuasa H, et al. J Clin Endocrinol Metab. 1993 Sep;77(3):600-4. doi: 10.1210/jcem.77.3.8103767. J Clin Endocrinol Metab. 1993. PMID: 8103767
Detection of a novel arginine vasopressin defect by dideoxy fingerprinting.
Krishnamani MR, Phillips JA 3rd, Copeland KC. Krishnamani MR, et al. J Clin Endocrinol Metab. 1993 Sep;77(3):596-8. doi: 10.1210/jcem.77.3.8370681. J Clin Endocrinol Metab. 1993. PMID: 8370681
Familial neurohypophyseal diabetes insipidus associated with a signal peptide mutation.
McLeod JF, Kovács L, Gaskill MB, Rittig S, Bradley GS, Robertson GL. McLeod JF, et al. J Clin Endocrinol Metab. 1993 Sep;77(3):599A-599G. doi: 10.1210/jcem.77.3.8370682. J Clin Endocrinol Metab. 1993. PMID: 8370682