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Homozygosity mapping of autosomal recessive demyelinating Charcot-Marie-Tooth neuropathy (CMT4H) to a novel locus on chromosome 12p11.21-q13.11. [electronic resource] by
- De Sandre-Giovannoli, A
- Delague, V
- Hamadouche, T
- Chaouch, M
- Krahn, M
- Boccaccio, I
- Maisonobe, T
- Chouery, E
- Jabbour, R
- Atweh, S
- Grid, D
- Mégarbané, A
- Lévy, N
Producer: 20060331
In:
Journal of medical genetics vol. 42
Availability: No items available.
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