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65.
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66.
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67.
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Myosin VIIA gene: heterogeneity of the mutations responsible for Usher syndrome type IB. [electronic resource] by
- Lévy, G
- Levi-Acobas, F
- Blanchard, S
- Gerber, S
- Larget-Piet, D
- Chenal, V
- Liu, X Z
- Newton, V
- Steel, K P
- Brown, S D
- Munnich, A
- Kaplan, J
- Petit, C
- Weil, D
Producer: 19970326
In:
Human molecular genetics vol. 6
Availability: No items available.
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68.
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72.
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73.
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Retinal findings in pediatric patients with Usher syndrome Type 1 due to mutations in MYO7A gene. [electronic resource] by
- Subirà, Olaia
- Català-Mora, Jaume
- Díaz-Cascajosa, Jesús
- Padrón-Pérez, Noel
- Claveria, M A
- Coll-Alsina, Natalia
- Bonnet, Crystel
- Petit, Christine
- Caminal, J M
- Prat, Joan
Producer: 20210618
In:
Eye (London, England) vol. 34
Availability: No items available.
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74.
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75.
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76.
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A missense mutation in myosin VIIA prevents aminoglycoside accumulation in early postnatal cochlear hair cells. [electronic resource] by
- Richardson, G P
- Forge, A
- Kros, C J
- Marcotti, W
- Becker, D
- Williams, D S
- Thorpe, J
- Fleming, J
- Brown, S D
- Steel, K P
Producer: 20000627
In:
Annals of the New York Academy of Sciences vol. 884
Availability: No items available.
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77.
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78.
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PHR1, an integral membrane protein of the inner ear sensory cells, directly interacts with myosin 1c and myosin VIIa. [electronic resource] by
- Etournay, Raphaël
- El-Amraoui, Aziz
- Bahloul, Amel
- Blanchard, Stéphane
- Roux, Isabelle
- Pézeron, Guillaume
- Michalski, Nicolas
- Daviet, Laurent
- Hardelin, Jean-Pierre
- Legrain, Pierre
- Petit, Christine
Producer: 20051128
In:
Journal of cell science vol. 118
Availability: No items available.
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