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Fibrillin-1

Fibrillin-1

Protein found in humans.

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Readers' pathsAug 2026 – Oct 2026

Readers go next to

Share of the 591 clicks on its links

  1. Marfan syndrome

    Genetic disorder involving connective tissue.

    40%

  2. Weill–Marchesani syndrome

    Rare generic disorder.

    29%

  3. Marfanoid–progeroid–lipodystrophy syndrome

    Medical condition.

    8.6%

  4. MASS syndrome

    Medical condition.

    7.6%

  5. Fibrillin

    Protein family.

    5.9%

  6. Shprintzen–Goldberg syndrome

    Congenital medical condition.

    4.4%

  7. Chromosome 15

    Human chromosome.

    1.7%

  8. EGF-like domain

    Protein domain.

    1.7%

Readers come from

Share of the 548 readers arriving from another article

  1. Marfan syndrome

    Genetic disorder involving connective tissue.

    59%

  2. Lizzie Velásquez

    American motivational speaker and YouTuber (born 1989).

    12%

  3. Marfanoid–progeroid–lipodystrophy syndrome

    Medical condition.

    11%

  4. Fibrillin

    Protein family.

    7.3%

  5. Congenital contractural arachnodactyly

    Medical condition.

    4.9%

  6. Scheuermann's disease

    Skeletal disorder.

    4.7%