(Q28279809)

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

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title

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

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main subject

primary hyperoxaluria type I

1 reference

K Nishiyama

1

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T Funai

series ordinal

2

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R Katafuchi

series ordinal

3

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F Hattori

series ordinal

4

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K Onoyama

series ordinal

5

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A Ichiyama

series ordinal

6

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language of work or name

English

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publication date

15 May 1991

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published in

Biochemical and Biophysical Research Communications

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volume

176

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issue

3

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page(s)

1093-9

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Identifiers

DOI

10.1016/0006-291X(91)90396-O

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PubMed ID

2039493

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(Q28279809)

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

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