Concepedia

Publication | Open Access

Mutations in KLHL40 Are a Frequent Cause of Severe Autosomal-Recessive Nemaline Myopathy

DOIFull Paper Access

220

Citations

34

References

2013

Year

Gianina Ravenscroft, Satoko Miyatake, Vilma‐Lotta Lehtokari, Emily J. Todd, Pauliina Vornanen, Kyle S. Yau, Yukiko Hayashi, Noriko Miyake, Yoshinori Tsurusaki, Hiroshi Doi,
The American Journal of Human Genetics

References

YearCitations

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