Connexin32 gene mutations in X-linked dominant Charcot-Marie-Tooth disease (CMTX1) - Concepedia

Concepedia

Publication | Open Access

Connexin32 gene mutations in X-linked dominant Charcot-Marie-Tooth disease (CMTX1)

DOI Full Paper Access

58

Citations

17

References

1997

Year

Emiel A. M. Janssen, Stephan Kemp, Gerard W. Hensels, Ongie G. Sie, Christine de Die‐Smulders, Jessica E. Hoogendijk, Marianne de Visser, Pieter A. Bolhuis

Mendelian DisorderConnexin32 Gene MutationsMedicineGeneticsPathogenesisGenetic DisorderPathologyMolecular GeneticsDisease Gene IdentificationMolecular Diagnostics

References

	Year	Citations

Page 1

Page 1