Guest guest Posted January 13, 2001 Report Share Posted January 13, 2001 Will read this one, its from the site you sent I followed the links like you said, thi sis interesting as it says, " It is suggested that Gln333Pro represents a rare disease-causing mutation, which results in the CMT2 phenotype " . ~>Becky M. Am J Hum Genet 2000 Jul;67(1):37-46 Related Articles, Books, OMIM, LinkOut [Click here to read] A new variant of Charcot-Marie-Tooth disease type 2 is probably the result of a mutation in the neurofilament-light gene. http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmg=Retrive Quote Link to comment Share on other sites More sharing options...
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