Relative risks for comorbidities associated with myotonic dystrophy: A population-based analysis.

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Congenital and childhood-onset myotonic dystrophy: importance of long-term data in natural history.Hypothyroid myopathy: A peculiar clinical presentation of thyroid failure. Review of the literature.

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Relative risks for comorbidities associated with myotonic dystrophy: A population-based analysis.

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Relative risks for comorbiditi ...... : A population-based analysis.

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Relative risks for comorbiditi ...... : A population-based analysis.

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Relative risks for comorbiditi ...... : A population-based analysis.

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Relative risks for comorbiditi ...... : A population-based analysis.

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Relative risks for comorbiditi ...... : A population-based analysis.

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Relative risks for comorbiditi ...... : A population-based analysis.

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Relative risks for comorbiditi ...... : A population-based analysis.

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Diana Abbott

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Lisa A Cannon-Albright

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Nicholas E Johnson

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P2860

Confirmation of the type 2 myotonic dystrophy (CCTG)n expansion mutation in patients with proximal myotonic myopathy/proximal myotonic dystrophy of different European origins: a single shared haplotype indicates an ancestral founder effect.

Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3' end of a transcript encoding a protein kinase family member.

Population frequency of myotonic dystrophy: higher than expected frequency of myotonic dystrophy type 2 (DM2) mutation in Finland.

Utah family-based analysis: past, present and future.

Myotonic dystrophy: from bench to bedside.

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659-661

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scholarly article

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10.1002/MUS.24766

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2015-07-14T00:00:00Z

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Relative risks for comorbidities associated with myotonic dystrophy: A population-based analysis.

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P2860

P2860

Relative risks for comorbidities associated with myotonic dystrophy: A population-based analysis.

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