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A telomerase component is defective in the human disease dyskeratosis congenita

โœ Scribed by Collins, Kathleen; Mitchell, James R.; Wood, Emily


Book ID
109832291
Publisher
Nature Publishing Group
Year
1999
Tongue
English
Weight
225 KB
Volume
402
Category
Article
ISSN
0028-0836

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Dyskeratosis congenita is a progressive bone-marrow failure syndrome that is characterized by abnormal skin pigmentation, leukoplakia and nail dystrophy 1,2 . X-linked, autosomal recessive and autosomal dominant inheritance have been found in different pedigrees. The X-linked form of the disease is