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561.
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562.
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563.
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Identification of an agrin mutation that causes congenital myasthenia and affects synapse function. [electronic resource] by
- Huzé, Caroline
- Bauché, Stéphanie
- Richard, Pascale
- Chevessier, Frédéric
- Goillot, Evelyne
- Gaudon, Karen
- Ben Ammar, Asma
- Chaboud, Annie
- Grosjean, Isabelle
- Lecuyer, Heba-Aude
- Bernard, Véronique
- Rouche, Andrée
- Alexandri, Nektaria
- Kuntzer, Thierry
- Fardeau, Michel
- Fournier, Emmanuel
- Brancaccio, Andrea
- Rüegg, Markus A
- Koenig, Jeanine
- Eymard, Bruno
- Schaeffer, Laurent
- Hantaï, Daniel
Producer: 20090923
In:
American journal of human genetics vol. 85
Availability: No items available.
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564.
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Quantitative and qualitative alterations of heparan sulfate in fibrogenic liver diseases and hepatocellular cancer. [electronic resource] by
- Tátrai, Péter
- Egedi, Krisztina
- Somorácz, Aron
- van Kuppevelt, Toin H
- Ten Dam, Gerdy
- Lyon, Malcolm
- Deakin, Jon A
- Kiss, András
- Schaff, Zsuzsa
- Kovalszky, Ilona
Producer: 20100503
In:
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society vol. 58
Availability: No items available.
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