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Clinical Case Study: CONNEXIN 32 MUTATION IN A TURKISH FAMILY WITH X-LINKED CHARCOT-MARIE-TOOTH DISEASE
SAHIN, NILUFER, TAN, MELIHA, KALAY, ERSAN, CALAPOGLU, MUSTAFA, KARAGUZEL, AHMETVolume:
113
Language:
english
Journal:
International Journal of Neuroscience
DOI:
10.1080/00207450390200972
Date:
January, 2003
File:
PDF, 177 KB
english, 2003