Mutations in BCAP31 Cause a Severe X-Linked Phenotype with Deafness, Dystonia, and Central Hypomyelination and Disorganize the Golgi Apparatus - Concepedia

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Mutations in BCAP31 Cause a Severe X-Linked Phenotype with Deafness, Dystonia, and Central Hypomyelination and Disorganize the Golgi Apparatus

DOI Full Paper Access

67

Citations

15

References

2013

Year

Pierre Cacciagli, Julie Sutera-Sardo, Ana Borges-Correia, Jean‐Christophe Roux, Imen Dorboz, Jean‐Pierre Desvignes, Catherine Badens, Marc Délepine, Mark Lathrop, Pierre Cau,

The American Journal of Human Genetics

Golgi ApparatusBcap31 CauseNeurobiology Of DiseaseMendelian DisorderNeurological DisorderGenetic DisorderGeneticsDegenerative DiseaseSocial SciencesNeurologyNeuroscienceCentral Nervous SystemNeuropathologyMedicineSevere X-linked Phenotype

References

	Year	Citations

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