A novel PMP22 mutation Ser22Phe in a family with hereditary neuropathy with liability to pressure palsies and CMT1A phenotypes - Concepedia

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A novel PMP22 mutation Ser22Phe in a family with hereditary neuropathy with liability to pressure palsies and CMT1A phenotypes

21

Citations

27

References

2004

Year

Kleopas A. Kleopa, Domna-Maria Georgiou, Paschalis Nicolaou, Pantelitsa Koutsou, Eleftherios S. Papathanasiou, Theodoros Kyriakides, Kyproula Christodoulou

Hereditary NeuropathyGenetic DisorderGeneticsCmt1a PhenotypesProgressive Supranuclear PalsyNeurologyNeuropathologyMedicineNeurogenetics

References

	Year	Citations

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