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Novel C3 mutation associated with MPGN2/DDD in a multiple-affected pedigree

✍ Scribed by Rubén Martínez-Barricarte; Francisco Valdés Cañedo; Tamara Montes; Agustín Tortajada; Sheila Pinto; Margarita López-Trascasa; Claire L. Harris; Santiago Rodríguez de Córdoba


Book ID
116757468
Publisher
Elsevier Science
Year
2009
Tongue
English
Weight
73 KB
Volume
46
Category
Article
ISSN
0161-5890

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