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A point mutation in glycoprotein IX coding sequence (Cys73 (TGT) to Tyr(TAT)) causes impaired surface expression of GPIb/IX/V complex in two families with Bernard-Soulier syndrome. [electronic resource] by
- Noda, M
- Fujimura, K
- Takafuta, T
- Shimomura, T
- Fujii, T
- Katsutani, S
- Fujimoto, T
- Kuramoto, A
- Yamazaki, T
- Mochizuki, T
- Matsuzaki, M
- Sano, M
Producer: 19970312
In:
Thrombosis and haemostasis vol. 76
Availability: No items available.
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Replication study for associations between polymorphisms in the CLDN5 and DGCR2 genes in the 22q11 deletion syndrome region and schizophrenia. [electronic resource] by
- Ishiguro, Hiroki
- Imai, Keiko
- Koga, Minori
- Horiuchi, Yasue
- Inada, Toshiya
- Iwata, Nakao
- Ozaki, Norio
- Ujike, Hiroshi
- Itokawa, Masanari
- Kunugi, Hiroshi
- Sasaki, Tsukasa
- Watanabe, Yuichiro
- Someya, Toshiyuki
- Arinami, Tadao
Producer: 20081114
In:
Psychiatric genetics vol. 18
Availability: No items available.
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