Prenatal molecular diagnosis of severe ornithine carbamoyltransferase deficiency due to a novel mutation, E181G

A. K. Topaloglu, C. Sansaricq, J. E. Fox, A. E. Bale, M. Tuchman, R. J. Desnick

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

1 Scopus citations

Original language	English
Pages (from-to)	82-83
Number of pages	2
Journal	Journal of Inherited Metabolic Disease
Volume	22
Issue number	1
DOIs	https://doi.org/10.1023/A:1005411601985
State	Published - 1999

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title = "Prenatal molecular diagnosis of severe ornithine carbamoyltransferase deficiency due to a novel mutation, E181G",

author = "Topaloglu, {A. K.} and C. Sansaricq and Fox, {J. E.} and Bale, {A. E.} and M. Tuchman and Desnick, {R. J.}",

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AU - Bale, A. E.

AU - Tuchman, M.

AU - Desnick, R. J.

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