Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Text availability
Article attribute
Article type
Publication date

Search Results

362 results
Filters applied: . Clear all Results are displayed in a computed author sort order. Results by year timeline is unavailable
Page 1
Molecular basis of apparent isolated 17,20-lyase deficiency: compound heterozygous mutations in the C-terminal region (Arg(496)----Cys, Gln(461)----Stop) actually cause combined 17 alpha-hydroxylase/17,20-lyase deficiency.
Yanase T, Waterman MR, Zachmann M, Winter JS, Simpson ER, Kagimoto M. Yanase T, et al. Among authors: waterman mr. Biochim Biophys Acta. 1992 Aug 25;1139(4):275-9. doi: 10.1016/0925-4439(92)90100-2. Biochim Biophys Acta. 1992. PMID: 1515452
362 results