Clinical, Functional and Genetic Analysis of Twenty-Four Patients with Chronic Granulomatous Disease – Identification of Eight Novel Mutations in CYBB and NCF2 Genes
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B. Conrad | M. Callanan | J. Stéphan | I. Durieu | H. Chambost | O. Hermine | K. Posfay-Barbe | J. Brion | S. Blanche | C. Coutton | C. Martel | P. Bordigoni | Z. Havlicekova | V. Satre | A. Salmon | A. Pagnier | M. Stasia | D. Plantaz | Michelle Mollin | Sylvain Beaumel | G. Vieville | C. Lefebvre | C. Bost-Bru | L. Eitenschenck | D. Floret | C. Galambrun | G. Michel | N. Blot | H. Rubié | G. Pouessel | S. Drillon-Haus | Tamara Voskresenky-Baricic | Kelecic Jadranka | M. Arriazu | Luis Alberto Garcia | L. Mansour | Gérard Michel | K. Posfay‐Barbe | Nathalie Blot | Stephanie Drillon-Haus | Cécile Martel