A novel mutation in the GRHPR gene in a Japanese patient with primary hyperoxaluria type 2.

A novel mutation in the GRHPR gene in a Japanese patient with primary hyperoxaluria type 2. Research Abstract Details 

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A novel mutation in the GRHPR gene in a Japanese patient with primary hyperoxaluria type 2. Abstract Text:

Tatsuya Takayama,Masao Nagata,Seiichiro Ozono,Katsuya Nonomura,Scott D Cramer,

A novel mutation in the GRHPR gene in a Japanese patient with primary hyperoxaluria type 2. Publishing Authors By Initials

T Takayama,M Nagata,S Ozono,K Nonomura,SD Cramer,

For similar genetic phenomena: phenotype research abstracts see: genetic phenomena: phenotype research

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A novel mutation in the GRHPR gene in a Japanese patient with primary hyperoxaluria type 2. Journal Published:

PUBLICATION TYPE: Research Support, N.I.H., Extr

Journal: Nephrology, dialysis, transplantation : official p

VOLUME: 22

Page Numbers: 2371-4

Journal Abbreviation: Nephrol. Dial. Transplant.

ISSN: 0931-0509

DAY: 17

MONTH: 05

YEAR: 2007

A novel mutation in the GRHPR gene in a Japanese patient with primary hyperoxaluria type 2. Information

Number of References:

LANGUAGE: eng

NlmUniqueID: 8706402

A novel mutation in the GRHPR gene in a Japanese patient with primary hyperoxaluria type 2. Keywords Mesh Terms:

KEYWORDS: Phenotype

MESH TERMS: genetics

Chemical & Substance for Abstract: A novel mutation in the GRHPR gene in a Japanese patient with primary hyperoxaluria type 2. Information

Substance Name: glyoxylate reductase

Registry Number: EC 1.1.1.26

Grant and Affiliation Information for A novel mutation in the GRHPR gene in a Japanese patient with primary hyperoxaluria type 2.

AFFILIATION: Department of Cancer Biology, Wake Forest University School of Medicine, Medical Center Blvd, Winston-Salem, NC 27157, USA. ttakayam@hama-med.ac.jp

Country: England

AGENCY: United States NIDDK

GRANT: DK069331

ACRONYM: DK

MEDLINETA: Nephrol Dial Transplant

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