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Dahl N
Uppsala University - Uppsala / Sweden
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AD Scientific Index ID: 1170632
Uppsala Universitet
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Dahl N's MOST POPULAR ARTICLES
1-)
A gene encoding a liver-specific ABC transporter is mutated in progressive familial intrahepatic cholestasisSS Strautnieks, LN Bull, AS Knisely, SA Kocoshis, N Dahl, H Arnell, ...Nature genetics 20 (3), 233-238, 199811201998
2-)
The gene encoding ribosomal protein S19 is mutated in Diamond-Blackfan anaemiaN Draptchinskaia, P Gustavsson, B Andersson, M Pettersson, TN Willig, ...Nature genetics 21 (2), 169-175, 19999431999
3-)
A gene mutated in X–linked myotubular myopathy defines a new putative tyrosine phosphatase family conserved in yeastJ Laporte, LJ Hu, C Kretz, JL Mandel, P Kioschis, JF Coy, SM Klauck, ...Nature genetics 13 (2), 175-182, 19966701996
4-)
HAX1 deficiency causes autosomal recessive severe congenital neutropenia (Kostmann disease)C Klein, M Grudzien, G Appaswamy, M Germeshausen, I Sandrock, ...Nature genetics 39 (1), 86-92, 20075992007
5-)
Diagnosing and treating Diamond Blackfan anaemia: results of an international clinical consensus conferenceA Vlachos, S Ball, N Dahl, BP Alter, S Sheth, U Ramenghi, J Meerpohl, ...British journal of haematology 142 (6), 859-876, 2008574*2008
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