SMC1A truncated mutations (causing loss of gene function)

Clinical trials for SMC1A truncated mutations (causing loss of gene function) explained in plain language.

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Coordination of rare diseases at sanford

Recruiting now

The Coordination of Rare Diseases at Sanford (CoRDS) is an international patient registry that serves as a centralized resource for rare disease research. Individuals affected by rare diseases, undiagnosed conditions, and disorders of unknown prevalence may voluntarily contribute…

Matched conditions: SMC1A TRUNCATED MUTATIONS (CAUSING LOSS OF GENE FUNCTION)

Sponsor: Sanford Health

Last updated Oct 30, 2026 00:00 UTC

SMC1A truncated mutations (causing loss of gene function)

Get alerted when new SMC1A truncated mutations (causing loss of gene function) trials appear

Coordination of rare diseases at sanford