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Mutation in the gene encoding lysosomal acid phosphatase (Acp2) causes cerebellum and skin malformation in mouse
Authors:Ashraf?U.?Mannan,Elena?Roussa,Cornelia?Kraus,Micheal?Rickmann,Joerg?Maenner,Karim?Nayernia,Kerstin?Krieglstein,André?Reis,Wolfgang?Engel  author-information"  >  author-information__contact u-icon-before"  >  mailto:wengel@gwdg.de"   title="  wengel@gwdg.de"   itemprop="  email"   data-track="  click"   data-track-action="  Email author"   data-track-label="  "  >Email author
Affiliation:(1) Institute of Human Genetics, University of Goettingen, Heinrich-Dueker-Weg 12, 37073 Goettingen, Germany;(2) Center of Anatomy, University of Goettingen, Kreuzbergring 36, 37075, Germany;(3) Institute of Human Genetics, University of Erlangen-Nuremberg, Schwabachanlage 10, 91054 Erlangen, Germany
Abstract:
Keywords:Mutant mouse strain  Genetic linkage  Cerebellum  Hair follicle  Lysosomal storage diseases
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