Dominant Mutations in KBTBD13, a Member of the BTB/Kelch Family, Cause Nemaline Myopathy with Cores - Concepedia

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Dominant Mutations in KBTBD13, a Member of the BTB/Kelch Family, Cause Nemaline Myopathy with Cores

DOI Full Paper Access

157

Citations

20

References

2010

Year

Nyamkhishig Sambuughin, Kyle S. Yau, Montse Olivé, Rachael M. Duff, Munkhuu Bayarsaikhan, Shajia Lu, Laura González, Padma Sivadorai, Kristen L. Nowak, Gianina Ravenscroft,

The American Journal of Human Genetics

Genetic DisorderGeneticsPathologyMolecular GeneticsCause Nemaline MyopathyMedicineBtb/kelch FamilyDominant Mutations

References

	Year	Citations

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