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Multiple identification of a particular type of hereditary C1q deficiency in the Turkish population: review of the cases and additional genetic and functional analysis

✍ Scribed by F. Petry; A. Izzet Berkel; Michael Loos


Publisher
Springer
Year
1997
Tongue
English
Weight
149 KB
Volume
100
Category
Article
ISSN
0340-6717

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