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

✍ Scribed by A. K. Topaloglu; C. Sansaricq; J. E. Fox; A. E. Bale; M. Tuchman; R. J. Desnick

• Book ID: 110224547
• Publisher: Springer
• Year: 1999
• Tongue: English
• Weight: 35 KB
• Volume: 22
• Category: Article
• ISSN: 0141-8955
• DOI: 10.1023/a:1005411601985