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Volumn 220, Issue 3, 1996, Pages 1036-1042
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A case of male-limited precocious puberty caused by a point mutation in the second transmembrane domain of the luteinizing hormone choriogonadotropin receptor gene
a,e b c d e a |
Author keywords
[No Author keywords available]
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Indexed keywords
ADENYLATE CYCLASE;
CHORIONIC GONADOTROPIN RECEPTOR;
CYCLIC AMP;
CYTOSINE;
INOSITOL PHOSPHATE;
LUTEINIZING HORMONE RECEPTOR;
METHIONINE;
PHOSPHOLIPASE C;
THREONINE;
THYMINE;
AMINO ACID SUBSTITUTION;
ANIMAL CELL;
ARTICLE;
BINDING AFFINITY;
CASE REPORT;
CONTROLLED STUDY;
ENZYME ACTIVITY;
GENETIC TRANSFECTION;
HUMAN;
HUMAN CELL;
JAPAN;
LEYDIG CELL;
MALE;
NONHUMAN;
NUCLEIC ACID BASE SUBSTITUTION;
POINT MUTATION;
PRECOCIOUS PUBERTY;
PRESCHOOL CHILD;
PRIORITY JOURNAL;
PROTEIN CONFORMATION;
PROTEIN DOMAIN;
RECEPTOR BINDING;
RECEPTOR GENE;
ANIMALIA;
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EID: 0029992481
PISSN: 0006291X
EISSN: None
Source Type: Journal
DOI: 10.1006/bbrc.1996.0528 Document Type: Article |
Times cited : (53)
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References (17)
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