Gain-of-function mutations in TRPV4 cause autosomal dominant brachyolmia

Gain-of-function mutations in TRPV4 cause autosomal dominant brachyolmia is a paper indexed in ScholarIQ from OpenAlex.

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Gain-of-function mutations in TRPV4 cause autosomal dominant brachyolmia has 236 citations in the OpenAlex counts ScholarIQ stores.

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Gain-of-function mutations in TRPV4 cause autosomal dominant brachyolmia has 2008 year in the ScholarIQ index.

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Gain-of-function mutations in TRPV4 cause autosomal dominant brachyolmia has bronze oa status in the ScholarIQ index.

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