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Volumn 39, Issue 1, 2012, Pages 91-94
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CYP7B1 mutations in French-Canadian hereditary spastic paraplegia subjects.
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Author keywords
[No Author keywords available]
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Indexed keywords
CYP7B1 PROTEIN, HUMAN;
STEROID MONOOXYGENASE;
ARTICLE;
CANADA;
ETHNOLOGY;
FAMILY HEALTH;
FEMALE;
GENE FREQUENCY;
GENETICS;
GENOTYPE;
HEREDITARY MOTOR SENSORY NEUROPATHY;
HUMAN;
MALE;
MUTATION;
NUCLEOTIDE SEQUENCE;
ONSET AGE;
AGE OF ONSET;
CANADA;
DNA MUTATIONAL ANALYSIS;
FAMILY HEALTH;
FEMALE;
GENE FREQUENCY;
GENOTYPE;
HUMANS;
MALE;
MUTATION;
SPASTIC PARAPLEGIA, HEREDITARY;
STEROID HYDROXYLASES;
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EID: 84858411577
PISSN: 03171671
EISSN: None
Source Type: Journal
DOI: 10.1017/S0317167100012774 Document Type: Article |
Times cited : (5)
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References (0)
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