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Cures Cures - connecting health & science MAR 23 Atelosteogenesis Type 2 by David Reynolds  /  5d Zuletzt aktualisiert am 22. March 2023 von David Reynolds Introduction Atelosteogenesis type 2 is a rare genetic disorder that affects skeletal development. It belongs to a group of genetic conditions known as skeletal dysplasias, which are characterized by abnormal bone growth and development. Atelosteogenesis type 2 is caused by mutations in the SLC26A2 gene and is inherited in an autosomal dom Atelosteogenesis Type 1 by David Reynolds  /  5d Zuletzt aktualisiert am 22. March 2023 von David Reynolds Introduction Atelosteogenesis type 1 is a rare genetic disorder that affects bone and cartilage development in the body. The condition is caused by mutations in the SLC26A2 gene, which provides instructions for making a protein called sulfate transporter. This protein is involved in the formation of cartilage and bone. Atelosteogenesis typ Ataxia with Vitamin E Deficien...

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