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ISPD gene mutations are a common cause of congenital and limb-girdle muscular dystrophies. [electronic resource] by
- Cirak, Sebahattin
- Foley, Aileen Reghan
- Herrmann, Ralf
- Willer, Tobias
- Yau, Shu
- Stevens, Elizabeth
- Torelli, Silvia
- Brodd, Lina
- Kamynina, Alisa
- Vondracek, Petr
- Roper, Helen
- Longman, Cheryl
- Korinthenberg, Rudolf
- Marrosu, Gianni
- Nürnberg, Peter
- Michele, Daniel E
- Plagnol, Vincent
- Hurles, Matt
- Moore, Steven A
- Sewry, Caroline A
- Campbell, Kevin P
- Voit, Thomas
- Muntoni, Francesco
Producer: 20130423
In:
Brain : a journal of neurology vol. 136
Availability: No items available.
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Impaired viability of muscle precursor cells in muscular dystrophy with glycosylation defects and amelioration of its severe phenotype by limited gene expression. [electronic resource] by
- Kanagawa, Motoi
- Yu, Chih-Chieh
- Ito, Chiyomi
- Fukada, So-ichiro
- Hozoji-Inada, Masako
- Chiyo, Tomoko
- Kuga, Atsushi
- Matsuo, Megumi
- Sato, Kanoko
- Yamaguchi, Masahiko
- Ito, Takahito
- Ohtsuka, Yoshihisa
- Katanosaka, Yuki
- Miyagoe-Suzuki, Yuko
- Naruse, Keiji
- Kobayashi, Kazuhiro
- Okada, Takashi
- Takeda, Shin'ichi
- Toda, Tatsushi
Producer: 20140131
In:
Human molecular genetics vol. 22
Availability: No items available.
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