Concepedia

Publication | Closed Access

Limb-Girdle Muscular Dystrophy Due to Emerin Gene Mutations

DOI

40

Citations

11

References

2007

Year

Shigehisa Ura, Yukiko Hayashi, Kanako Goto, Mina Astejada, Terumi Murakami, Masako Nagato, Shigeru Ohta, Yasuhisa Daimon, Hidehiro Takekawa, Koichi Hirata,
Archives of Neurology

Abstract

Mutations in EMD may indicate a limb-girdle muscular dystrophy phenotype. Identification of emerin deficiency among patients with limb-girdle muscular dystrophy is essential to prevent cardiac catastrophe.

References

YearCitations

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