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Mapping of a new locus for autosomal recessive demyelinating Charcot-Marie-Tooth disease to 19q13.1-13.3 in a large consanguineous Lebanese family: exclusion of MAG as a candidate gene. [electronic resource] by
- Delague, V
- Bareil, C
- Tuffery, S
- Bouvagnet, P
- Chouery, E
- Koussa, S
- Maisonobe, T
- Loiselet, J
- Mégarbané, A
- Claustres, M
Producer: 20000807
In:
American journal of human genetics vol. 67
Availability: No items available.
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