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Cardiac conduction defects associate with mutations in SCN5A. [electronic resource] by
- Schott, J J
- Alshinawi, C
- Kyndt, F
- Probst, V
- Hoorntje, T M
- Hulsbeek, M
- Wilde, A A
- Escande, D
- Mannens, M M
- Le Marec, H
Producer: 19990923
In:
Nature genetics vol. 23
Availability: No items available.
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38.
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Novel SCN5A mutation leading either to isolated cardiac conduction defect or Brugada syndrome in a large French family. [electronic resource] by
- Kyndt, F
- Probst, V
- Potet, F
- Demolombe, S
- Chevallier, J C
- Baro, I
- Moisan, J P
- Boisseau, P
- Schott, J J
- Escande, D
- Le Marec, H
Producer: 20020111
In:
Circulation vol. 104
Availability: No items available.
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39.
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[Genetic aspects of valvulopathies]. [electronic resource] by
- Kyndt, F
- Le Scouarnec, S
- Jaafar, P
- Gueffet, J-P
- Legendre, A
- Trochu, J-N
- Jousseaume, V
- Chaventré, A
- Schott, J-J
- Le Marec, H
- Probst, V
Producer: 20080328
In:
Archives des maladies du coeur et des vaisseaux vol. 100
Availability: No items available.
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40.
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Valvular dystrophy associated filamin A mutations reveal a new role of its first repeats in small-GTPase regulation. [electronic resource] by
- Duval, D
- Lardeux, A
- Le Tourneau, T
- Norris, R A
- Markwald, R R
- Sauzeau, V
- Probst, V
- Le Marec, H
- Levine, R
- Schott, J J
- Merot, J
Producer: 20140320
In:
Biochimica et biophysica acta vol. 1843
Availability: No items available.
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