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Autosomal recessive familial neurohypophyseal diabetes insipidus with continued secretion of mutant weakly active vasopressin -- Willcutts et al. 8 (7): 1303 -- Human Molecular Genetics - Details
Link Details
Peptide Station » Listing Details
| ID: | 282 |
| Title: | Autosomal recessive familial neurohypophyseal diabetes insipidus with continued secretion of mutant weakly active vasopressin -- Willcutts et al. 8 (7): 1303 -- Human Molecular Genetics - http://hmg.oxfordjournals.org/cgi/content/full/8/7/1303 |
| Pagerank: | N/A |
| Description: | UT, untranslated region; S, signal peptide; V, vasopressin peptide; N, neurophysin II; C, copeptin. Arrows with letters denote primers for PCR or sequencing ... |
| Category: | Peptide Families: Vasopressin Peptides |
| Link Owner: | pepadmin |
| Date Added: | August 30, 2006 11:25:48 PM |
| Number Hits: | 1 |