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Novel missense mutations outside the allosteric domain of glutamate dehydrogenase are prevalent in European patients with the congenital hyperinsulinism-hyperammonemia syndrome

✍ Scribed by René Santer; Martina Kinner; Marie Passarge; Andrea Superti-Furga; Ertan Mayatepek; Thomas Meissner; Reinhard Schneppenheim; Jürgen Schaub


Book ID
106136308
Publisher
Springer
Year
2001
Tongue
English
Weight
129 KB
Volume
108
Category
Article
ISSN
0340-6717

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