A novel point mutation in PMP22 gene associated with a familial case of Charcot-Marie-Tooth disease type 1A with sensorineural deafness - Concepedia

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A novel point mutation in PMP22 gene associated with a familial case of Charcot-Marie-Tooth disease type 1A with sensorineural deafness

24

Citations

13

References

2004

Year

In Soo Joo, Chang‐Seok Ki, Sung Joo, Kyoon Huh, Jong‐Won Kim

Neuromuscular Disorders

Mendelian DisorderGenetic DisorderGeneticsPathogenesisPathologyNovel Point MutationMolecular GeneticsDisease Gene IdentificationSensorineural DeafnessMedicinePmp22 Gene

References

	Year	Citations

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