What is Marfan syndrome?
Mutations in the FBN1 or fibrillin gene on chromosome 15 cause a genetic disorder called Marfan syndrome. The misshapen protein from the mutated gene weakens the tendons, ligaments and other connective tissues in the body.
tendons ligaments,chromosome 15,connective tissues,genetic disorder,mutations,protein
- ID: 15955
- Source: DNALC.DNAi
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