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Article

A patient with slowly progressive adult-onset nemaline myopathy and novel compound heterozygous mutations in the nebulin gene.

Journal of the neurological sciences - 15 Feb 2017

Tsunoda Keiichiro, Yamashita Toru, Motokura Emi, Takahashi Yoshiaki, Sato Kota, Takemoto Mami, Hishikawa Nozomi, Ohta Yasuyuki, Nishikawa Atsuko, Nishino Ichizo, Abe Koji

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Share to Diagnosis, Differential
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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Muscle Proteins

Share to Muscle Weakness

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Share to Myopathies, Nemaline

Share to Respiratory Insufficiency

Source

Identifiers

PMID: 28131200
DOI: 10.1016/j.jns.2016.12.069

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Related research

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A patient with slowly progressive adult-onset nemaline myopathy and novel compound heterozygous mutations in the nebulin gene.PMID 28131200Read ↗

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