Dominant Intermediate Charcot-Marie-Tooth Neuropathy Maps to Chromosome 19p12-p13.2

The hereditary disorders of peripheral nerve form one of the most common groups of human genetic diseases, collectively called Charcot-Marie-Tooth (CMT) neuropathy. Using linkage analysis we have identified a new locus for a form of CMT that we have called “dominant intermediate CMT” (DI-CMT). A gen...

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Main Authors: Kennerson, M. L., Zhu, D., Gardner, R. J. M., Storey, E., Merory, J., Robertson, S. P., Nicholson, G. A.
Formáid: Artigo
Teanga:Inglês
Foilsithe: The American Society of Human Genetics 2001
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Report
Rochtain Ar Líne:https://ncbi.nlm.nih.gov/pmc/articles/PMC1226074/
https://ncbi.nlm.nih.gov/pubmed/11533912
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