Phenotypic heterogeneity of marfan-like connective tissue disorders associated with mutations in the transforming growth factor-β receptor genes

Circulation Journal

Volumn 71, Issue 8, 2007, Pages 1305-1309

  Akutsu, Koichi ^a   Morisaki, Hiroko ^a   Takeshita, Satoshi ^a   Sakamoto, Shingo ^a   Tamori, Yuiichi ^a   Yoshimuta, Tsuyoshi ^a   Yokoyama, Naoyuki ^a   Nonogi, Hiroshi ^a   Ogino, Hitoshi ^a   Morisaki, Takayuki ^a  

^a NATIONAL CEREBRAL AND CARDIOVASCULAR CENTER   (Japan)

Author keywords

Loeys Dietz syndrome; Marfan syndrome; Marfan like connective tissue disorder; Receptor genes; Transforming growth factor

Indexed keywords

TRANSFORMING GROWTH FACTOR BETA RECEPTOR; TRANSFORMING GROWTH FACTOR BETA RECEPTOR 1; TRANSFORMING GROWTH FACTOR BETA RECEPTOR 2;

ADULT; AORTA DISSECTION; ARTICLE; CLINICAL ARTICLE; CLINICAL EXAMINATION; CLINICAL FEATURE; CONNECTIVE TISSUE DISEASE; DISEASE ASSOCIATION; FEMALE; FURLONG SYNDROME; GENE MUTATION; GENETIC HETEROGENEITY; HUMAN; LOEYS DIETZ SYNDROME; MALE; MARFAN SYNDROME; PHENOTYPE; RECEPTOR GENE; SPHRINTZEN GOLDBERG SYNDROME; SYNDROME;

ADULT; COLLAGEN TYPE III; CONNECTIVE TISSUE DISEASES; DNA MUTATIONAL ANALYSIS; FEMALE; HUMANS; MALE; MARFAN SYNDROME; MICROFILAMENT PROTEINS; MUTATION; PHENOTYPE; PROTEIN-SERINE-THREONINE KINASES; RECEPTORS, TRANSFORMING GROWTH FACTOR BETA;

EID: 34547590052     PISSN: 13469843     EISSN: 13474820     Source Type: Journal    
DOI: 10.1253/circj.71.1305     Document Type: Article

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