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Roque Carrero-Valenzuela Selected Research

Gap Junction beta-1 Protein

6/2013Hereditary motor and sensory neuropathy (HMSN) type X1 in an Argentinean family reveals independent GJB1/Cx32 mutations at the identical nucleotide position.

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Roque Carrero-Valenzuela Research Topics

Disease

1Charcot-Marie-Tooth Disease (Peroneal Muscular Atrophy)
06/2013
1Hereditary Sensory and Motor Neuropathy (Dejerine Sottas Disease)
06/2013

Drug/Important Bio-Agent (IBA)

1Gap Junction beta-1 ProteinIBA
06/2013
1NucleotidesIBA
06/2013