Primary hyperoxaluria type I due to a point mutation of T...

Biochemical and Biophysical Research Communications 1991 Vol. 176; Iss. 3

Primary hyperoxaluria type I due to a point mutation of T to C in the coding region of the serine:pyruvate aminotransferase gene

Kozo Nishiyama, Tsuneyoshi Funai, Ritsuko Katafuchi, Fumitada Hattori, Kaoru Onoyama, Arata Ichiyama
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Volume:
176
Year:
1991
Language:
english
Pages:
1100
DOI:
10.1016/0006-291x(91)90396-o
File:
PDF, 929 KB
english, 1991
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