CMTM8-v2 |
CMTX4 |
PLAP-1 |
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this term refers to a recessive intermediate variant of Charcot-Marie-Tooth disease, which is caused by compound heterozygous mutation in the gene encoding lysyl-tRNA synthetase.
For other proteins (or fragments thereof) with at least one additional activity that differs from the established 'classical' activity of the parent protein see also: Dual identity proteins and Cryptides MiniCOPE Dictionary.
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