The fibrillinopathies: New insights with focus on the paradigm of opposing phenotypes for both FBN1 and FBN2.

Journal Information

Full Title: Hum Mutat

Abbreviation: Hum Mutat

Country: Unknown

Publisher: Unknown

Language: N/A

Publication Details

Subject Category: Genetics, Medical

Available in Europe PMC: Yes

Available in PMC: Yes

PDF Available: No

Transparency Score
2/6
33.3% Transparent
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Core Indicators
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COI Disclosure
Evidence found in paper:

"S. Peeters (12X5422N) and J. A. N. Meester (12X8520N) are postdoctoral FWO (Fund for Scientific Research Flanders) fellows. B. L. Loeys holds a consolidator grant from the European Research Council (Genomia—ERC‐COG‐2017‐771945)."

Protocol Registration
Open Access
Paper is freely available to read
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Assessment Info

Tool: rtransparent

OST Version: N/A

Last Updated: Aug 05, 2025