Mutations in the tuberous sclerosis complex gene TSC2 are a cause of sporadic pulmonary lymphangioleiomyomatosis

Proceedings of the National Academy of Sciences of the United States of America

Volumn 97, Issue 11, 2000, Pages 6085-6090

  Carsillo, Thomas ^a   Astrinidis, Aristotelis ^a   Henske, Elizabeth Petri ^a  

^a FOX CHASE CANCER CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANGIOMYOLIPOMA; ARTICLE; CLINICAL ARTICLE; CONTROLLED STUDY; DISEASE ASSOCIATION; FEMALE; GENE MUTATION; HETEROZYGOSITY LOSS; HUMAN; HUMAN CELL; HUMAN TISSUE; INTERSTITIAL LUNG DISEASE; KIDNEY TUMOR; LYMPHANGIOLEIOMYOMATOSIS; LYMPHOBLASTOID CELL; PRIORITY JOURNAL; SOMATIC MUTATION; TUBEROUS SCLEROSIS;

ADULT; CELL TRANSFORMATION, NEOPLASTIC; DNA MUTATIONAL ANALYSIS; DNA, NEOPLASM; FEMALE; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; HUMANS; KIDNEY; LUNG NEOPLASMS; LYMPHANGIOLEIOMYOMATOSIS; MUSCLE, SMOOTH; NEOPLASTIC SYNDROMES, HEREDITARY; POINT MUTATION; REPRESSOR PROTEINS; SEQUENCE DELETION; TUBEROUS SCLEROSIS; TUMOR SUPPRESSOR PROTEINS;

EID: 0034705207     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.97.11.6085     Document Type: Article

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