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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.
Am J Hum Genet. 2000 Jul;67(1):236-43. doi: 10.1086/302980. Epub 2000 Jun 2.
Am J Hum Genet. 2000.
PMID: 10848494
Free PMC article.
Reciprocal expression of myelin-associated glycoprotein splice variants in the adult human peripheral and central nervous systems.
Miescher GC, Lützelschwab R, Erne B, Ferracin F, Huber S, Steck AJ.
Miescher GC, et al.
Brain Res Mol Brain Res. 1997 Dec 15;52(2):299-306. doi: 10.1016/s0169-328x(97)00254-4.
Brain Res Mol Brain Res. 1997.
PMID: 9495552
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