Autosomal dominant nemaline myopathy: A new phenotype unlinked to previously known genetic loci - Concepedia

Concepedia

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Autosomal dominant nemaline myopathy: A new phenotype unlinked to previously known genetic loci

16

Citations

18

References

2006

Year

P.Y. Jeannet, L. Mittaz, M. Dunand, Johannes Alexander Lobrinus, Luisa Bonafé, Thierry Küntzer

Neuromuscular Disorders

Rare DiseasesNew PhenotypeAutoimmune DiseaseMendelian DisorderGenetic DisorderGeneticsPathologyDegenerative DiseaseDisease Gene IdentificationMedicineGenetic LociClinical Genetics

References

	Year	Citations

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