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Volumn 37, Issue 1, 2005, Pages 68-71
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Mutation screening of Cx32 in Han Chinese patients with Charcot-Marie-Tooth disease.
a a a a a a a a a a a |
Author keywords
[No Author keywords available]
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Indexed keywords
CONNEXIN 32;
GAP JUNCTION PROTEIN;
ARTICLE;
CHINA;
ETHNOLOGY;
FEMALE;
GENETICS;
HEREDITARY MOTOR SENSORY NEUROPATHY;
HUMAN;
MALE;
OPEN READING FRAME;
PEDIGREE;
POINT MUTATION;
X CHROMOSOME;
CHARCOT-MARIE-TOOTH DISEASE;
CHINA;
CONNEXINS;
FEMALE;
HUMANS;
MALE;
OPEN READING FRAMES;
PEDIGREE;
POINT MUTATION;
X CHROMOSOME;
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EID: 39049183553
PISSN: 1671167X
EISSN: None
Source Type: Journal
DOI: None Document Type: Article |
Times cited : (8)
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References (0)
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