Sandbox Reserved 1103: Difference between revisions
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=== Dyskeratosis congenita === | === Dyskeratosis congenita === | ||
The unifying features Dyskeratosis congenita (DC) is a disorder which is | The unifying features Dyskeratosis congenita (DC) is a disorder which is characterised by bone marrow dysfunction, abnormality of the skin, mucocutaneous triad of oral leucoplakia, nail dystrophy, as well as a predisposition to cancer. | ||
TIN2 is one of the nine identified genes that when mutated are related to the Dyskeratosis congenita, the others being DKC1, TERC, TERT, NOP10, NHP2, TIN2, C16orf57, TCAB1 and PARN. | TIN2 is one of the nine identified genes that when mutated are related to the Dyskeratosis congenita, the others being DKC1, TERC, TERT, NOP10, NHP2, TIN2, C16orf57, TCAB1 and PARN. | ||
