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

✍ Scribed by Sibylle Jakubiczka; Thomas Bettecken; Klaus Mohnike; Reinhard Schneppenheim; Markus Stumm; Holger Tönnies; Marianne Volleth; Peter Wieacker


Publisher
Springer
Year
2006
Tongue
English
Weight
116 KB
Volume
166
Category
Article
ISSN
0340-6997

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