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Adult-onset krabbe's disease in siblings with novel mutations in the galactocerebrosidase gene.
Issues in Law and Medicine.
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Clinical phenotypes of different MPZ (P
0) mutations may include Charcot-Marie-Tooth type 1B, Dejerine-Sottas, and congenital hypomyelination. Neuron. 1996 Academic Article GET IT
Times cited: 315