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XB-ANAT-412
Papers associated with tooth (and gja5)
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Null mutations of connexin32 in patients with X-linked Charcot-Marie-Tooth disease., Bruzzone R., Neuron. November 1, 1994; 13 (5): 1253-60. |
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Connexin32 mutations associated with X-linked Charcot-Marie-Tooth disease show two distinct behaviors: loss of function and altered gating properties., Ressot C., J Neurosci. June 1, 1998; 18 (11): 4063-75. |
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Biological functions of connexin genes revealed by human genetic defects, dominant negative approaches and targeted deletions in the mouse., Willecke K., Novartis Found Symp. January 1, 1999; 219 76-88; discussion 88-96. |
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