I-cell disease-like phenotype in mice deficient in mannose 6-phosphate receptors

Transgenic Research

Volumn 7, Issue 6, 1998, Pages 473-483

  Dittmer, Frank ^a   Hafner, Angela ^b   Ulbrich, Eva J ^a   Moritz, JÖrg D ^a   Schmidt, Peter ^b   Schmahl, Wolfgang ^b   Pohlmann, Regina ^a   Figura, Kurt V ^a  

^a UNIVERSITY OF GÖTTINGEN   (Germany)

^b UNIVERSITY OF MUNICH   (Germany)

Author keywords

I cell disease; Imprinting; Lysosomal enzyme sorting; Lysosome biogenesis; Mannose 6 phosphate

Indexed keywords

ALLELE; BRAIN; CROSSING; DWARFISM; FACIAL DYSPLASIA; FIBROBLAST; GENETIC TRAIT; INHERITANCE; LIVER; LYSOSOME; MOUSE; PHENOTYPE; SOMATOMEDIN B RECEPTOR;

ANIMALS; BLOTTING, WESTERN; BONE AND BONES; FEMALE; GENOMIC IMPRINTING; GENOTYPE; HETEROZYGOTE; LYSOSOMES; MALE; MICE; MUCOLIPIDOSES; PHENOTYPE; RECEPTOR, IGF TYPE 2;

EID: 0032214329     PISSN: 09628819     EISSN: None     Source Type: Journal    
DOI: 10.1023/A:1008823315416     Document Type: Article

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