Congenital adrenal hyperplasia due to 21-hydroxylase deficiency is a common autosomal recessive disorder (MIM# 201910) due to mutations in the 21-hydroxylase (CYP21) gene (GDB Accession # M12792). Using our protocol for single strand conformational polymorphism (SSCP) analysis, we have identified tw
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Identification ofTrypanosoma cruzisublineages by the simple method of single-stranded conformation DNA polymorphism (SSCP)
โ Scribed by Hiroo Higo; Sachio Miura; Takeshi Agatsuma; Tatsuyuki Mimori; Tetsuo Yanagi; Moritoshi Iwagami; A. Rojas de Arias; Vivian Matta; Kenji Hirayama; Tsutomu Takeuchi; Isao Tada; Kunisuke Himeno
- Book ID
- 106128431
- Publisher
- Springer-Verlag
- Year
- 2006
- Tongue
- English
- Weight
- 258 KB
- Volume
- 100
- Category
- Article
- ISSN
- 1432-1955
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