Mutation in the gene encoding lysosomal acid phosphatase (Acp2) causes cerebellum and skin malformation in mouse

Neurogenetics

Volumn 5, Issue 4, 2004, Pages 229-238

  Mannan, Ashraf U ^a   Roussa, Elena ^a   Kraus, Cornelia ^b   Rickmann, Micheal ^a   Maenner, Joerg ^a   Nayernia, Karim ^a   Krieglstein, Kerstin ^a   Reis, André ^b   Engel, Wolfgang ^a  

^a UNIVERSITY OF GÖTTINGEN   (Germany)

^b UNIVERSITY OF ERLANGEN NUREMBERG   (Germany)

Author keywords

Cerebellum; Genetic linkage; Hair follicle; Lysosomal storage diseases; Mutant mouse strain

Indexed keywords

LYSOSOME ACID PHOSPHATASE; PHOSPHATASE; UNCLASSIFIED DRUG;

ANIMAL TISSUE; ARTICLE; BRAIN CORTEX; BRAIN MALFORMATION; CEREBELLUM DISEASE; CHROMOSOME 2; GENE MUTATION; GENETIC TRANSCRIPTION; GRANULE CELL; HAIR FOLLICLE; HISTOLOGY; HOMEOSTASIS; HOMOZYGOTE; LYSOSOME; LYSOSOME STORAGE DISEASE; MISSENSE MUTATION; MOUSE; NONHUMAN; PRIORITY JOURNAL; PURKINJE CELL; SKIN MANIFESTATION; ULTRASTRUCTURE;

AMINO ACID SEQUENCE; ANIMALS; CEREBELLAR ATAXIA; CEREBELLUM; HAIR FOLLICLE; ISOENZYMES; LINKAGE (GENETICS); LYSOSOMES; MICE; MICE, INBRED C57BL; MICE, NEUROLOGIC MUTANTS; MICROSCOPY, ELECTRON; MOLECULAR SEQUENCE DATA; NEURONS; PHENOTYPE; PROTEIN-TYROSINE-PHOSPHATASE; SKIN ABNORMALITIES; STRUCTURE-ACTIVITY RELATIONSHIP;

ATAXIA;

EID: 12944320332     PISSN: 13646745     EISSN: None     Source Type: Journal    
DOI: 10.1007/s10048-004-0197-9     Document Type: Article

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