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JMG.35.7.590
JMG.35.7.590
http://dx.doi.org/10.1136/JMG.35.7.590
Mutation analysis of the nerve specific promoter of the peripheral myelin protein 22 gene in CMT1 disease and HNPP.
P356
Q33681015-5F5CF952-5D91-46E2-B8B5-87BED2319CB1
P356
JMG.35.7.590
http://dx.doi.org/10.1136/JMG.35.7.590