Publication | Closed Access
Peripheral myelin protein–22 gene maps in the duplication in chromosome 17p11.2 associated with Charcot–Marie–Tooth 1A
294
Citations
21
References
1992
Year
Mendelian DisorderGenetic DisorderGeneticsMolecular GeneticsCharcot–marie–tooth 1AMedicineCell BiologyChromosome 22NeurogeneticsChromosome 17P11.2
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