An Indian child with Kindler syndrome resulting from a new homozygous nonsense mutation (C468X) in the KIND1 gene (Q81609038)
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scientific article published on 01 May 2005
Language | Label | Description | Also known as |
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English | An Indian child with Kindler syndrome resulting from a new homozygous nonsense mutation (C468X) in the KIND1 gene |
scientific article published on 01 May 2005 |
Statements
An Indian child with Kindler syndrome resulting from a new homozygous nonsense mutation (C468X) in the KIND1 gene (English)
Sethuraman G
Fassihi H
Ashton GH
Bansal A
Kabra M