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Fanny Rostedt

1PUBLICATIONS

5CO-AUTHORS

Neurology and neuromuscular diseases

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|May 21, 2025

A homozygous single-nucleotide variant in <i>TNNT1</i> causes abnormal troponin T isoform expression in a patient with severe nemaline myopathy: A case report.

Milla Laarne, Ali Oghabian, Jenni Laitila

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Milla Laarne

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Ali Oghabian

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Lydia Sagath

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Vilma-Lotta Lehtokari

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Katarina Pelin

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Milla Laarne

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Ali Oghabian

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Lydia Sagath

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Vilma-Lotta Lehtokari

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