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Select article: Expanding the spectrum of TNNC2 variants in neonatal hypotonia - a family report of a homozygous loss-of-function variant

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Case report

First published November, 2025

Expanding the spectrum of TNNC2 variants in neonatal hypotonia - a family report of a homozygous loss-of-function variant

Anthony Maino, Marie Chevallier, Diane Giovannini [...]

Journal of Neuromuscular Diseases

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