Symptomatic ornithine carbamoyltransferase deficiency (point mutation H202P) with normal in vitro activity

M. Staudt; B. Wermuth; P. Freisinger; A. Hässler; B. F. Pontz

doi:10.1023/A:1005315531630

Symptomatic ornithine carbamoyltransferase deficiency (point mutation H202P) with normal in vitro activity

M. Staudt
, B. Wermuth
, P. Freisinger
, A. Hässler
, B. F. Pontz

Department of Pediatric Medicine

Technical University of Munich
Children's Hospital
Inselspital Universitatsspital

Research output: Contribution to journal › Article › peer-review

7 Scopus citations

Original language	English
Pages (from-to)	71-72
Number of pages	2
Journal	Journal of Inherited Metabolic Disease
Volume	21
Issue number	1
DOIs	https://doi.org/10.1023/A:1005315531630
State	Published - 1998

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title = "Symptomatic ornithine carbamoyltransferase deficiency (point mutation H202P) with normal in vitro activity",

author = "M. Staudt and B. Wermuth and P. Freisinger and A. H{\"a}ssler and Pontz, \{B. F.\}",

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AU - Staudt, M.

AU - Wermuth, B.

AU - Freisinger, P.

AU - Hässler, A.

AU - Pontz, B. F.

PY - 1998

Y1 - 1998

UR - https://www.scopus.com/pages/publications/0031985733

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JO - Journal of Inherited Metabolic Disease

JF - Journal of Inherited Metabolic Disease

IS - 1

ER -

Symptomatic ornithine carbamoyltransferase deficiency (point mutation H202P) with normal in vitro activity

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