Symptoms of OTC deficiency but not DMD in a female carrier of an Xp21.1 deletion including the genes for dystrophin and OTC

Author: Jakubiczka Sibylle   Bettecken Thomas   Mohnike Klaus   Schneppenheim Reinhard   Stumm Markus   Tönnies Holger   Volleth Marianne   Wieacker Peter  

Publisher: Springer Publishing Company

ISSN: 0340-6199

Source: European Journal of Pediatrics, Vol.166, Iss.7, 2007-07, pp. : 743-745

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