In the progeny of somatic cell hybrids formed by fusion of human lymphocytes and Chinese hamster mutant cells, a single human chromosome A2 was selectively retained when grown in appropriate medium. Spontaneous breakage of this chromosome in different hybrid subclones led to the assignment of the ge
โฆ LIBER โฆ
Chromosome Assignment of the Human Gene for Galactose-1-phosphate Uridyltransferase
โ Scribed by N. C. Sun, C. C. Chang and E. H. Y. Chu
- Book ID
- 123651859
- Publisher
- National Academy of Sciences
- Year
- 1974
- Tongue
- English
- Weight
- 992 KB
- Volume
- 71
- Category
- Article
- ISSN
- 0027-8424
- DOI
- 10.2307/62784
No coin nor oath required. For personal study only.
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## Communicated by Alastair Brown Classical galactosemia is an autosomal recessive disorder caused by mutations in the galactose-1-phosphate uridyltransferase (GALT) gene. Our group developed a disease-specific database containing all of the reported sequence variants in GALT (Available at: http:/
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