Results
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13241.
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13242.
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13243.
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13244.
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13245.
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13246.
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Long-read sequence analysis of the MECP2 gene in Rett syndrome patients: correlation of disease severity with mutation type and location. [electronic resource] by
- Cheadle, J P
- Gill, H
- Fleming, N
- Maynard, J
- Kerr, A
- Leonard, H
- Krawczak, M
- Cooper, D N
- Lynch, S
- Thomas, N
- Hughes, H
- Hulten, M
- Ravine, D
- Sampson, J R
- Clarke, A
Producer: 20000623
In:
Human molecular genetics vol. 9
Availability: No items available.
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13247.
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Hailey-Hailey disease is caused by mutations in ATP2C1 encoding a novel Ca(2+) pump. [electronic resource] by
- Sudbrak, R
- Brown, J
- Dobson-Stone, C
- Carter, S
- Ramser, J
- White, J
- Healy, E
- Dissanayake, M
- Larrègue, M
- Perrussel, M
- Lehrach, H
- Munro, C S
- Strachan, T
- Burge, S
- Hovnanian, A
- Monaco, A P
Producer: 20000623
In:
Human molecular genetics vol. 9
Availability: No items available.
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13248.
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13249.
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13250.
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13251.
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13252.
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13253.
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13254.
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13255.
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13256.
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13257.
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13258.
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13259.
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13260.
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