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Volumn 37, Issue 1, 2005, Pages 100-105
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Molecular genetics of Charcot-Marie-Tooth disease
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Author keywords
[No Author keywords available]
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Indexed keywords
MEMBRANE PROTEIN;
MTMR2 PROTEIN, HUMAN;
MYELIN PROTEIN;
NEUROFILAMENT PROTEIN;
NEUROFILAMENT PROTEIN L;
PERIAXIN;
PMP22 PROTEIN, HUMAN;
PROTEIN TYROSINE PHOSPHATASE;
ANIMAL;
CHROMOSOME 17;
GENE DELETION;
GENETICS;
HEREDITARY MOTOR SENSORY NEUROPATHY;
HUMAN;
POINT MUTATION;
REVIEW;
ANIMALS;
CHARCOT-MARIE-TOOTH DISEASE;
CHROMOSOMES, HUMAN, PAIR 17;
GENE DELETION;
HUMANS;
MEMBRANE PROTEINS;
MYELIN PROTEINS;
NEUROFILAMENT PROTEINS;
POINT MUTATION;
PROTEIN-TYROSINE-PHOSPHATASE;
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EID: 34548058036
PISSN: 1671167X
EISSN: None
Source Type: Journal
DOI: None Document Type: Review |
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Times cited : (2)
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References (48)
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