✦ LIBER ✦
Gene screening in Japanese families with complete deficiency of thyroxine-binding globulin demonstrates that a nucleotide deletion at codon 352 may be a race specific mutation
✍ Scribed by K. Takeda; K. Iyota; Y. Mori; Y. Tamura; T. Suehlro; Y. Kubo; S. Refetoff; K. Hashimoto
- Book ID
- 114719895
- Publisher
- John Wiley and Sons
- Year
- 1994
- Tongue
- English
- Weight
- 580 KB
- Volume
- 40
- Category
- Article
- ISSN
- 0300-0664
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