A common genetic variant of luteinizing hormone; relation to normal and aberrant pituitary-gonadal function

European Journal of Pharmacology

Volumn 414, Issue 1, 2001, Pages 1-7

  Lamminen, Tarja ^a   Huhtaniemi, Ilpo ^a  

^a UNIVERSITY OF TURKU   (Finland)

Author keywords

[No Author keywords available]

Indexed keywords

LUTEINIZING HORMONE DERIVATIVE;

AMINO ACID SUBSTITUTION; GENE MUTATION; GENETIC VARIABILITY; HUMAN; HYPOPHYSIS GONAD SYSTEM; PATHOPHYSIOLOGY; POINT MUTATION; PRIORITY JOURNAL; REVIEW; SIGNAL TRANSDUCTION; SUBFERTILITY;

ANIMALS; EXONS; FEMALE; GENE FREQUENCY; GLYCOPROTEIN HORMONES, ALPHA SUBUNIT; GONADS; HUMANS; LUTEINIZING HORMONE; MALE; MUTATION, MISSENSE; OBESITY; PITUITARY GLAND; POINT MUTATION; POLYCYSTIC OVARY SYNDROME; POLYMORPHISM, GENETIC; RECEPTORS, LH;

EID: 0035936874     PISSN: 00142999     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0014-2999(01)00756-7     Document Type: Review

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