Kathleen Patterson

Pediatrics

4800 Sand Point Way NE
Seattle, WA 98105

Last Updated: 09/26/2026

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Found 1 publications

A novel missense mutation in POMT1 modulates the severe congenital muscular dystrophy phenotype associated with POMT1 nonsense mutations.

A novel missense mutation in POMT1 modulates the severe congenital muscular dystrophy phenotype associated with POMT1 nonsense mutations.

Journal: Neuromuscular disorders : NMD

Published: September 28, 2013

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Last Updated: 09/26/2026