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ArticleNeurology2012

Exome sequencing identifies a novel TRPV4 mutation in a CMT2C family.

Guida Landouré et al.PubMed ↗Full text ↗Publisher ↗

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17 papers cite it

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The trial

NCT06677502500 enrolled2024
Full record →Abstract, authors, funding and every citing paper · PMID 22675077