Exome sequencing as a diagnostic tool to identify a causal mutation in genetically highly heterogeneous limb-girdle muscular dystrophy

Tohru Matsuura; Tatsuaki Kurosaki; Yoshio Omote; Narihiro Minami; Yukiko K. Hayashi; Ichizo Nishino; Koji Abe

doi:10.1038/jhg.2013.33

Exome sequencing as a diagnostic tool to identify a causal mutation in genetically highly heterogeneous limb-girdle muscular dystrophy

Tohru Matsuura, Tatsuaki Kurosaki, Yoshio Omote, Narihiro Minami, Yukiko K. Hayashi, Ichizo Nishino, Koji Abe

Research output: Contribution to journal › Letter

Original language	English
Pages (from-to)	564-565
Number of pages	2
Journal	Journal of Human Genetics
Volume	58
Issue number	8
DOIs	https://doi.org/10.1038/jhg.2013.33
Publication status	Published - Aug 1 2013

ASJC Scopus subject areas

Genetics
Genetics(clinical)

Cite this

Matsuura, T., Kurosaki, T., Omote, Y., Minami, N., Hayashi, Y. K., Nishino, I., & Abe, K. (2013). Exome sequencing as a diagnostic tool to identify a causal mutation in genetically highly heterogeneous limb-girdle muscular dystrophy. Journal of Human Genetics, 58(8), 564-565. https://doi.org/10.1038/jhg.2013.33

Exome sequencing as a diagnostic tool to identify a causal mutation in genetically highly heterogeneous limb-girdle muscular dystrophy. / Matsuura, Tohru; Kurosaki, Tatsuaki; Omote, Yoshio; Minami, Narihiro; Hayashi, Yukiko K.; Nishino, Ichizo; Abe, Koji.

In: Journal of Human Genetics, Vol. 58, No. 8, 01.08.2013, p. 564-565.

Research output: Contribution to journal › Letter

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Access to Document

10.1038/jhg.2013.33