McCune-Albright syndrome: Molecular genetics

Journal of Pediatric Endocrinology and Metabolism

Volumn 15, Issue SUPPL. 3, 2002, Pages 875-882

  Lumbroso, Serge ^a   Paris, Françoise ^a   Sultan, Charles ^a  

^a LAPEYRONIE HOSPITAL   (France)

Author keywords

Activating mutation; G protein; McCune Albright syndrome; Molecular genetics; Precious puberty

Indexed keywords

ADENYLATE CYCLASE; ARGININE; CYSTEINE; GROWTH HORMONE; HISTIDINE; PROTEIN SUBUNIT; STIMULATORY GUANINE NUCLEOTIDE BINDING PROTEIN; DNA; GUANINE NUCLEOTIDE BINDING PROTEIN;

ADRENAL HYPERPLASIA; ALBRIGHT SYNDROME; AMINO ACID SUBSTITUTION; ARTICLE; BONE DYSPLASIA; CAFE AU LAIT SPOT; CHILD; CONTROLLED STUDY; DEVELOPMENTAL STAGE; DISEASE ASSOCIATION; DISEASE SEVERITY; ENDOCRINE DISEASE; ENZYME ACTIVITY; FEMALE; GOITER; GROWTH HORMONE RELEASE; HORMONE SYNTHESIS; HUMAN; HYPOPHYSIS ADENOMA; HYPOTHESIS; MAJOR CLINICAL STUDY; MALE; MOLECULAR GENETICS; MOSAICISM; POLYMERASE CHAIN REACTION; PRECOCIOUS PUBERTY; SIGNAL TRANSDUCTION; SKIN DEFECT; SOMATIC MUTATION; ZYGOTE; GENETICS; MOLECULAR BIOLOGY; PATHOPHYSIOLOGY; REVIEW;

CHILD; DNA; FEMALE; FIBROUS DYSPLASIA, POLYOSTOTIC; GTP-BINDING PROTEINS; HUMAN; MALE; MOLECULAR BIOLOGY; HUMANS;

EID: 0036045169     PISSN: 0334018X     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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