Ethnic-Specific WRN Mutations in South Asian Werner Syndrome Patients: Potential Founder Effect in Patients with Indian or Pakistani Ancestry.

Authors:
Saha B; Lessel D; Nampoothiri S; Rao AS; Hisama FM and 7 more

Journal:
Mol Genet Genomic Med

Publication Year: 2013

DOI:
10.1002/mgg3.1

PMCID:
PMC3736606

PMID:
23936869

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Journal Information

Full Title: Mol Genet Genomic Med

Abbreviation: Mol Genet Genomic Med

Country: Unknown

Publisher: Unknown

Language: N/A

Publication Details

Subject Category: Genetics, Medical

Available in Europe PMC: Yes

Available in PMC: Yes

PDF Available: No

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"Conflict of Interest None declared."

Evidence found in paper:

"Funding Information This study was supported by National Institutes of Health (NIH) grants, R24CA78088 (G. M. M./J. O.), R24AG42328 (G. M. M./J. O.), and R21AG33313 (J. O.), an Ellison Medical Foundation Senior Scholar Award (J. O.), and an American Heart Association fellowship (B. S.)."

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