Marfan syndrome

Julie De Backer, Maurice Godfrey

Research output: Chapter in Book/Report/Conference proceedingChapter

Abstract

Marfan syndrome is an autosomal, dominant, heritable disorder of connective tissue characterized by defects in the skeletal, ocular, and cardiovascular systems. Marfan syndrome is caused by mutations in the gene encoding fibrillin-1 ....

Original languageEnglish (US)
Title of host publicationxPharm
Subtitle of host publicationThe Comprehensive Pharmacology Reference
PublisherElsevier Inc.
Pages1-6
Number of pages6
ISBN (Print)9780080552323
DOIs
StatePublished - Jan 1 2007

Fingerprint

Marfan Syndrome
Cardiovascular System
Connective Tissue
Mutation
Genes
Fibrillin-1

ASJC Scopus subject areas

  • Pharmacology, Toxicology and Pharmaceutics(all)

Cite this

De Backer, J., & Godfrey, M. (2007). Marfan syndrome. In xPharm: The Comprehensive Pharmacology Reference (pp. 1-6). Elsevier Inc.. https://doi.org/10.1016/B978-008055232-3.60621-X

Marfan syndrome. / De Backer, Julie; Godfrey, Maurice.

xPharm: The Comprehensive Pharmacology Reference. Elsevier Inc., 2007. p. 1-6.

Research output: Chapter in Book/Report/Conference proceedingChapter

De Backer, J & Godfrey, M 2007, Marfan syndrome. in xPharm: The Comprehensive Pharmacology Reference. Elsevier Inc., pp. 1-6. https://doi.org/10.1016/B978-008055232-3.60621-X
De Backer J, Godfrey M. Marfan syndrome. In xPharm: The Comprehensive Pharmacology Reference. Elsevier Inc. 2007. p. 1-6 https://doi.org/10.1016/B978-008055232-3.60621-X
De Backer, Julie ; Godfrey, Maurice. / Marfan syndrome. xPharm: The Comprehensive Pharmacology Reference. Elsevier Inc., 2007. pp. 1-6
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