Inactivating PAPSS2 mutations in a patient with premature pubarche. [electronic resource]
Producer: 20090605Description: 2310-8 p. digitalISSN:- 1533-4406
- Androgens -- blood
- Androstenedione -- blood
- Child
- Dehydroepiandrosterone -- blood
- Diagnosis, Differential
- Female
- Heterozygote
- Humans
- Multienzyme Complexes -- deficiency
- Mutation
- Polycystic Ovary Syndrome -- diagnosis
- Puberty, Precocious -- blood
- RNA, Messenger -- metabolism
- Sequence Analysis, DNA
- Sulfate Adenylyltransferase -- deficiency
- Sulfotransferases -- blood
- Testosterone -- blood
No physical items for this record
Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
There are no comments on this title.
Log in to your account to post a comment.