Fanconi anemia with sun-sensitivity caused by a Xeroderma pigmentosum-associated missense mutation in XPF.

Autor: Popp, Isabell1 isabell.popp@uni-wuerzburg.de, Punekar, Maqsood2 Maqsood.puneka@lthtr.nhs.uk, Telford, Nick3 Nick.Telford@christie.nhs.uk, Stivaros, Stavros4,5 stavros.stivaros@manchester.ac.uk, Chandler, Kate5,6 Kate.Chandler@cmft.nhs.uk, Minnis, Meenakshi5,6 Meenakshi.Minnis@cmft.nhs.uk, Castleton, Anna7 Anna.castleton@christie.nhs.uk, Higham, Claire7,8 Claire.Higham@christie.nhs.uk, Hopewell, Louise7 Louise.Hopewell@Christie.nhs.uk, Gareth Evans, D.6 Gareth.Evans@cmft.nhs.uk, Raams, Anja9 j.raams@erasmusmc.nl, Theil, Arjan F.9 a.theil@erasmusmc.nl, Meyer, Stefan5,7,10,11,12 aisabell.popp@uni-wuerzburg.de, Schindler, Detlev1 bMaqsood.puneka@lthtr.nhs.uk
Zdroj: BMC Medical Genetics. 1/11/2018, Vol. 19, p1-N.PAG. 10p.
Databáze: Academic Search Ultimate
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