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Amyotrophic Lateral Sclerosis Volume 12, 2011 - Issue 3
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Research Article

The P413L chromogranin B variation in French patients with sporadic amyotrophic lateral sclerosis

Hélène Blasco UMR INSERM U930, Université François-Rabelais de Tours, France; Laboratoire de Biochimie et de Biologie Moléculaire, Hôpital Bretonneau, CHRU de Tours, Tours, FranceCorrespondence[email protected]
,
Philippe Corcia UMR INSERM U930, Université François-Rabelais de Tours, France; Centre SLA, Service de Neurologie et Neurophysiologie Clinique, CHRU de Tours, France
,
Charlotte Veyrat-Durebex Laboratoire de Biochimie et de Biologie Moléculaire, Hôpital Bretonneau, CHRU de Tours, Tours, France
,
Cathleen Coutadeur Laboratoire de Biochimie et de Biologie Moléculaire, Hôpital Bretonneau, CHRU de Tours, Tours, France
,
Clémentine Fournier Laboratoire de Biochimie et de Biologie Moléculaire, Hôpital Bretonneau, CHRU de Tours, Tours, France
,
William Camu Centre SLA, Hôpital Gui-de-Chauliac, CHU Montpellier, Montpellier, France
,
Paul Gordon Northern Navajo Medical Center, Shiprock, New Mexico, USA
,
Julien Praline UMR INSERM U930, Université François-Rabelais de Tours, France; Centre SLA, Service de Neurologie et Neurophysiologie Clinique, CHRU de Tours, France
,
Christian R. Andres UMR INSERM U930, Université François-Rabelais de Tours, France; Laboratoire de Biochimie et de Biologie Moléculaire, Hôpital Bretonneau, CHRU de Tours, Tours, France
,
Patrick Vourc'h UMR INSERM U930, Université François-Rabelais de Tours, France; Laboratoire de Biochimie et de Biologie Moléculaire, Hôpital Bretonneau, CHRU de Tours, Tours, France
& The French Als Study Group show all
Pages 210-214 | Received 02 Jul 2010, Accepted 05 Sep 2010, Published online: 11 Oct 2010

Citations (7)

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Read on this site (1)

Xinglong Yang, Shimei Li, Dongmei Xing, Peiyun Li, Ci Li, Ling Qi, Yanming Xu & Hui Ren. (2018) Lack of association between the P413L variant of chromogranin B and ALS risk or age at onset: a meta-analysis. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 19:1-2, pages 80-86.
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Articles from other publishers (6)

Georgios Pampalakis, Konstantinos Mitropoulos, Georgia Xiromerisiou, Efthymios Dardiotis, Georgia Deretzi, Maria Anagnostouli, Theodora Katsila, Michail Rentzos & George P. Patrinos. (2019) New molecular diagnostic trends and biomarkers for amyotrophic lateral sclerosis. Human Mutation 40:4, pages 361-373.
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Mehdi Ghasemi & Robert H. BrownJr.Jr.. (2018) Genetics of Amyotrophic Lateral Sclerosis. Cold Spring Harbor Perspectives in Medicine 8:5, pages a024125.
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Yasuyuki Ohta, Genevieve Soucy, Daniel Phaneuf, Jean-Nicolas Audet, François Gros-Louis, Guy A. Rouleau, Hélène Blasco, Philippe Corcia, Peter M. Andersen, Frida Nordin, Toru Yamashita, Koji Abe & Jean-Pierre Julien. (2016) Sex-dependent effects of chromogranin B P413L allelic variant as disease modifier in amyotrophic lateral sclerosis. Human Molecular Genetics, pages ddw304.
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Ricci Claudia, Battistini Stefania, Avemaria Francesca, Benigni Michele, Tarlarini Claudia, Giannini Fabio, Corbo Massimo, Lunetta Christian & Penco Silvana. (2015) Lack of relationship between the P413L chromogranin B variant and a SALS Italian cohort. Gene 568:2, pages 186-189.
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Beatrice Nefussy & Vivian E. Drory. 2013. Neurodegenerative Diseases: Integrative PPPM Approach as the Medicine of the Future. Neurodegenerative Diseases: Integrative PPPM Approach as the Medicine of the Future 205 233 .
Rune Østern, Toril Fagerheim, Kristin Ørstavik, Trygve Holmøy, Arvid Heiberg, Inger Lund-Petersen, Tim M. Strom, Øivind Nilssen & Arve Dahl. (2012) Hereditary motor neuron disease in a large Norwegian family with a “H46R” substitution in the superoxide dismutase 1 gene. Neuromuscular Disorders 22:6, pages 511-521.
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