Identification of two HEXA mutations causing infantile-onset Tay-Sachs disease in the Persian population
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概要
- 論文の詳細を見る
- 2011-09-01
著者
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Desnick Robert
Department Of Human Genetics Mount Sinai School Of Medicine
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Haghighi Alireza
Wellcome Trust Centre For Human Genetics University Of Oxford
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REZAZADEH Jamileh
Milad Genetics Clinic, Behzisti Organization
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SHADMEHRI Azam
Milad Genetics Clinic, Behzisti Organization
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HAGHIGHI Amirreza
The Hospital for Sick Children, University of Toronto
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KORNREICH Ruth
Department of Genetics and Genomic Sciences, Mount Sinai School of Medicine of New York University
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Kornreich Ruth
Department Of Genetics And Genomic Sciences Mount Sinai School Of Medicine Of New York University
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Shadmehri Azam
Milad Genetics Clinic Behzisti Organization
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Haghighi Amirreza
The Hospital For Sick Children University Of Toronto
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Rezazadeh Jamileh
Milad Genetics Clinic Behzisti Organization
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Desnick Robert
Department Of Genetics And Genomic Sciences Mount Sinai School Of Medicine Of New York University
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Hanghighi Alireza
Wellcome Trust Centre for Human Genetics, University of Oxford
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- Identification of two HEXA mutations causing infantile-onset Tay-Sachs disease in the Persian population