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Volumn 1, Issue 3, 2008, Pages 254-261
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Cilia, Alström syndrome--molecular mechanisms and therapeutic perspectives.
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Author keywords
[No Author keywords available]
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Indexed keywords
ALMS1 PROTEIN, HUMAN;
HUMAN GROWTH HORMONE;
PROTEIN;
ADULT;
ALSTROM SYNDROME;
BLINDNESS;
BODY MASS;
CASE REPORT;
CHROMOSOME 2;
EUKARYOTIC FLAGELLUM;
FEMALE;
GENETIC MARKER;
GENETICS;
GENOTYPE;
HEARING LOSS;
HUMAN;
INSULIN RESISTANCE;
MULTIPLE MALFORMATION SYNDROME;
MUTATION;
NON INSULIN DEPENDENT DIABETES MELLITUS;
OBESITY;
PHENOTYPE;
RETINITIS PIGMENTOSA;
REVIEW;
TREATMENT OUTCOME;
ABNORMALITIES, MULTIPLE;
ADULT;
ALSTROM SYNDROME;
BLINDNESS;
BODY MASS INDEX;
CHROMOSOMES, HUMAN, PAIR 2;
CILIA;
DIABETES MELLITUS, TYPE 2;
FEMALE;
GENETIC MARKERS;
GENOTYPE;
HEARING LOSS;
HUMAN GROWTH HORMONE;
HUMANS;
INSULIN RESISTANCE;
MUTATION;
OBESITY;
PHENOTYPE;
PROTEINS;
RETINITIS PIGMENTOSA;
TREATMENT OUTCOME;
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EID: 77449148006
PISSN: 1844122X
EISSN: None
Source Type: Journal
DOI: None Document Type: Review |
Times cited : (6)
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References (27)
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