Author:
Rudelius Martina,Osanger Andreas,Kohlmann Stephanie,Augustin Martin,Piontek Guido,Heinzmann Ulrich,Jennen Gisela,Russ Andreas,Matiasek Kaspar,Stumm Gabriele,Schlegel Juergen
Publisher
Springer Science and Business Media LLC
Subject
Cellular and Molecular Neuroscience,Neurology (clinical),Pathology and Forensic Medicine
Reference31 articles.
1. Augustin M, Sedlmeier R, Peters T, Huffstadt U, Kochmann E, Simon D, Schoniger M, Garke-Mayerthaler S, Laufs J, Mayhaus M, Franke S, Klose M, Graupner A, Kurzmann M, Zinser C, Wolf A, Voelkel M, Kellner M, Kilian M, Seelig S, Koppius A, Teubner A, Korthaus D, Nehls M, Wattler S (2005) Efficient and fast targeted production of murine models based on ENU mutagenesis. Mamm Genome 16:405–413
2. Barbosa MD, Nguyen QA, Tchernev VT (1996) Identification of the homologous beige and Chediak–Higashi syndrome genes. Nature 382:262–265
3. Cardoso C, Leventer RJ, Dowling JJ et al (2002) Clinical and molecular basis of classical lissencephaly: mutations in the LIS1 gene (PAFAH1B1). Hum Mutat 19:4–15
4. Certain S, Barrat F, Pastural E et al (2000) Protein truncation test of LYST reveals heterogenous mutations in patients with Chediak–Higashi syndrome. Blood 95:979–983
5. Fagerland JA, Hagemoser WA, Ireland WP (1987) Ultrastructure and stereology of leukocytes and platelets of normal foxes and a fox with a Chediak-Higashi-like syndrome. Vet Pathol 24:164–169
Cited by
32 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献