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Mutation in the gene encoding lysosomal acid phosphatase (Acp2) causes cerebellum and skin malformation in mouse |
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| Authors: | Ashraf?U.?Mannan,Elena?Roussa,Cornelia?Kraus,Micheal?Rickmann,Joerg?Maenner,Karim?Nayernia,Kerstin?Krieglstein,André?Reis,Wolfgang?Engel 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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