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A unique collaboration among Shriners Hospital for Children – Canada, CHU Sainte-Justine and 9IÖÆ×÷³§Ãâ·Ñ has enabled researchers to identify genetic mutations involved in a rare disease that causes scoliosis and bone malformations.

The findings, published in The American Journal of Human Genetics, are likely to help doctors recognize the genetic disease, and could someday lead to therapies for the condition.

Classified as: Shriner's Hospital for Children, genetic diseases, genetic mutations, medicine, children, CHU Sainte-Justine Research Center
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Published on: 2 Nov 2017
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