✦ LIBER ✦
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 17α-hydroxylase/17,20-lyase deficiency
✍ Scribed by Yanase, Toshihiko; Waterman, Michael R.; Zachmann, Milo; Winter, J.S.D.; Simpson, Evan R; Kagimoto, Masaaki
- Book ID
- 122893525
- Publisher
- Elsevier Science
- Year
- 1992
- Tongue
- English
- Weight
- 583 KB
- Volume
- 1139
- Category
- Article
- ISSN
- 0925-4439
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