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Volumn 23, Issue 2, 2000, Pages 147-149
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The challenge of CMTX and connexin 32 mutations
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Author keywords
[No Author keywords available]
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Indexed keywords
GAP JUNCTION PROTEIN;
EDITORIAL;
ELECTRODIAGNOSIS;
FAMILIAL DISEASE;
GENE MUTATION;
HEREDITARY MOTOR SENSORY NEUROPATHY;
HUMAN;
MUSCLE ACTION POTENTIAL;
MUSCLE WEAKNESS;
NERVE CONDUCTION;
NERVOUS SYSTEM ELECTROPHYSIOLOGY;
PRIORITY JOURNAL;
SCHWANN CELL;
X CHROMOSOMAL INHERITANCE;
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EID: 0033985679
PISSN: 0148639X
EISSN: None
Source Type: Journal
DOI: 10.1002/(sici)1097-4598(200002)23:2<147::aid-mus1>3.0.co;2-%23 Document Type: Editorial |
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Times cited : (12)
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References (14)
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