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- W1977579232 abstract "Fibroblasts have been developed from skin biopsies obtained from 3 children with type IV glycogen storage disease (amylopectinosis) and have been shown to be profoundly deficient in branching enzyme activity. Branching enzyme activity was reduced below control levels in both parents of one patient, supporting the previously suggested autosomal recessive inheritance. Fibroblasts cultured from normal amniotic fluid cells have branching activity similar to that of normal skin fibroblasts. Antenatal diagnosis of this uniformly fatal, untreatable disease should therefore be possible." @default.
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- W1977579232 date "1971-04-01" @default.
- W1977579232 modified "2023-10-16" @default.
- W1977579232 title "Type IV glycogen storage disease: Branching enzyme deficiency in skin fibroblasts and possible heterozygote detection" @default.
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- W1977579232 doi "https://doi.org/10.1016/s0022-3476(71)80466-3" @default.
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