A recessive mutation in beta-IV-spectrin (SPTBN4) associates with congenital myopathy, neuropathy, and central deafness - Concepedia

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A recessive mutation in beta-IV-spectrin (SPTBN4) associates with congenital myopathy, neuropathy, and central deafness

58

Citations

17

References

2017

Year

Ellen Knierim, Esther Gill, Franziska Seifert, Susanne Morales-Gonzalez, Sathya D. Unudurthi, Thomas J. Hund, Werner Stenzel, Markus Schuelke

Congenital MyopathyMendelian DisorderGenetic DisorderMedicineGeneticsPathologyCentral DeafnessCochlear DevelopmentNeuropathologyRecessive MutationNeurogenetics

References

	Year	Citations

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