Results
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1141.
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1142.
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1143.
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1144.
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1145.
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1147.
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1148.
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1149.
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1150.
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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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1151.
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1152.
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1153.
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1154.
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1155.
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Beta-sarcoglycan (A3b) mutations cause autosomal recessive muscular dystrophy with loss of the sarcoglycan complex. [electronic resource] by
- Bönnemann, C G
- Modi, R
- Noguchi, S
- Mizuno, Y
- Yoshida, M
- Gussoni, E
- McNally, E M
- Duggan, D J
- Angelini, C
- Hoffman, E P
Producer: 19951208
In:
Nature genetics vol. 11
Availability: No items available.
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1156.
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1157.
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Targeted inactivation of dystrophin gene product Dp71: phenotypic impact in mouse retina. [electronic resource] by
- Dalloz, Cécile
- Sarig, Rachel
- Fort, Patrice
- Yaffe, David
- Bordais, Agnès
- Pannicke, Thomas
- Grosche, Jens
- Mornet, Dominique
- Reichenbach, Andreas
- Sahel, José
- Nudel, Uri
- Rendon, Alvaro
Producer: 20040326
In:
Human molecular genetics vol. 12
Availability: No items available.
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1158.
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POMT1 mutation results in defective glycosylation and loss of laminin-binding activity in alpha-DG. [electronic resource] by
- Kim, D S
- Hayashi, Y K
- Matsumoto, H
- Ogawa, M
- Noguchi, S
- Murakami, N
- Sakuta, R
- Mochizuki, M
- Michele, D E
- Campbell, K P
- Nonaka, I
- Nishino, I
Producer: 20040719
In:
Neurology vol. 62
Availability: No items available.
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1159.
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1160.
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