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Novel C1q mutation in an homozygous C1q-deficienct patient affected of glomerulonephritis and Rothmund-Thomson Syndrome

✍ Scribed by Lopez-Lera, A.; Torres-Canizales, J.; Garrido, S.; Morales, A.; Lopez-Trascasa, M.


Book ID
123148512
Publisher
Elsevier Science
Year
2013
Tongue
English
Weight
70 KB
Volume
56
Category
Article
ISSN
0161-5890

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