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Ethnic-specific WRN mutations in South Asian Werner syndrome patients: potential founder effect in patients with Indian or Pakistani ancestry. Molecular Genetics & Genomic Medicine

Publication Type : Journal Article

Publisher : Molecular Genetics & Genomic Medicine, p. 7–14

Source : Molecular Genetics & Genomic Medicine, p. 7–14 (2013)

Campus : Kochi

School : School of Medicine

Department : Paediatrics

Verified : Yes

Year : 2013

Abstract :

Cite this Research Publication : B. Saha, Lessel, D., Nampoothiri, S., Rao, A. S., M, F., ,, Peter, D., Bennett, C., N€urnberg, G., N€urnberg, P., Martin, G. M., Kubisch, C., and Oshima, J., “Ethnic-specific WRN mutations in South Asian Werner syndrome patients: potential founder effect in patients with Indian or Pakistani ancestry. Molecular Genetics & Genomic Medicine”, Molecular Genetics & Genomic Medicine, pp. 7–14, 2013.

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