Whole-genome sequencing identifies a novel ABCB7 gene mutation for X-linked congenital cerebellar ataxia in a large family of Mongolian ancestry - Concepedia

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Publication | Open Access

Whole-genome sequencing identifies a novel ABCB7 gene mutation for X-linked congenital cerebellar ataxia in a large family of Mongolian ancestry

DOI Full Paper Access

29

Citations

42

References

2015

Year

Maria Protasova, Anastasia P. Grigorenko, T. V. Tyazhelova, Denis A. Reshetov, Fedor Gusev, Alexander E Laptenko, Andrey Goltsov, S. A. Klyushnikov

European Journal of Human Genetics

Mongolian AncestryMendelian DisorderGenetic DisorderGeneticsLarge FamilyMolecular BiologyMolecular GeneticsDisease Gene IdentificationGenomicsWhole-genome Sequencing IdentifiesMedicineClinical Genetics

References

	Year	Citations

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