Results
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Absence of keratin 19 in mice causes skeletal myopathy with mitochondrial and sarcolemmal reorganization. [electronic resource] by
- Stone, Michele R
- O'Neill, Andrea
- Lovering, Richard M
- Strong, John
- Resneck, Wendy G
- Reed, Patrick W
- Toivola, Diana M
- Ursitti, Jeanine A
- Omary, M Bishr
- Bloch, Robert J
Producer: 20080207
In:
Journal of cell science vol. 120
Availability: No items available.
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553.
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554.
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555.
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Mutations in B3GALNT2 cause congenital muscular dystrophy and hypoglycosylation of α-dystroglycan. [electronic resource] by
- Stevens, Elizabeth
- Carss, Keren J
- Cirak, Sebahattin
- Foley, A Reghan
- Torelli, Silvia
- Willer, Tobias
- Tambunan, Dimira E
- Yau, Shu
- Brodd, Lina
- Sewry, Caroline A
- Feng, Lucy
- Haliloglu, Goknur
- Orhan, Diclehan
- Dobyns, William B
- Enns, Gregory M
- Manning, Melanie
- Krause, Amanda
- Salih, Mustafa A
- Walsh, Christopher A
- Hurles, Matthew
- Campbell, Kevin P
- Manzini, M Chiara
- Stemple, Derek
- Lin, Yung-Yao
- Muntoni, Francesco
Producer: 20130729
In:
American journal of human genetics vol. 92
Availability: No items available.
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556.
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557.
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558.
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Expression of dystroglycan and the laminin-alpha 2 chain in the rat peripheral nerve during development. [electronic resource] by
- Masaki, Toshihiro
- Matsumura, Kiichiro
- Hirata, Akira
- Yamada, Hiroki
- Hase, Asako
- Arai, Ken
- Shimizu, Teruo
- Yorifuji, Hiroshi
- Motoyoshi, Kazuo
- Kamakura, Keiko
Producer: 20020328
In:
Experimental neurology vol. 174
Availability: No items available.
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559.
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560.
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