Clinical phenotype in X-linked Charcot-Marie-Tooth disease with an entire deletion of the connexin 32 coding sequence - Concepedia

Concepedia

Publication | Closed Access

Clinical phenotype in X-linked Charcot-Marie-Tooth disease with an entire deletion of the connexin 32 coding sequence

39

Citations

22

References

2001

Year

Masanori Nakagawa, Hiroshi Takashima, Fujio Umehara, Kimiyoshi Arimura, Fumio Miyashita, Norihiro Takenouchi, Wataru Matsuyama, Mitsuhiro Osame

Journal of the Neurological Sciences

Connexin 32GeneticsPathogenesisX-linked Charcot-marie-tooth DiseasePathologyClinical PhenotypeMedicineMolecular Medicine

References

	Year	Citations

Page 1