Studies on complementation of beta hexosaminidase deficiency in human GM2 gangliosidosis.

Complementation of beta hexosaminidase A (hex A) deficiency was obtained by Sendai virus-mediated somatic cell hybridization of cultured skin fibroblasts from two unrelated patients with Tay-Sachs disease (TSD) and one patient with Sandhoff-Jatzkewitz disease (SJD). The newly formed hex A was identi...

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Hlavní autoři: Rattazzi, M C, Brown, J A, Davidson, R G, Shows, T B
Médium: Artigo
Jazyk:Inglês
Vydáno: 1976
Témata:
Research Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC1684927/
https://ncbi.nlm.nih.gov/pubmed/817596
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