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G. Kurleman
G. Kurleman
Hereditary neuralgic amyotrophy
Cancer research
Septin
Gene
Biology
2
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2
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Mutations in the human septin 0 gene (SEPT9) cause hereditary neuralgic amyotrophy (HNA)
2005
Gregor Kuhlenbäumer
Mark C. Hannibal
Eva Nelis
Anja Schirmacher
Nathalie Verpoorten
J. Meuleman
Giles D. J. Watts
E. De Vriendt
Peter Young
Florian Stögbauer
Hartmut Halfter
Bg Betz
G. Kurleman
Thomas D. Bird
Eila M. Airaksinen
Tarja Mononen
A. Pou Serradell
Jm Prats
C. Van Broeckhoven
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Hemiatrophia faciei progressiva (Parry-Romberg-Syndrom)
1993
Monatsschrift Kinderheilkunde
E.-M. Menges-Wenzel
G. Kurleman
J. H. Pawlowitzki
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