Neurogenetics: Difference between revisions
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{{Journal | {{Journal | ||
|Title=Neurogenetics | |Title=[http://www.springer.com/biomed/neuroscience/journal/10048 Neurogenetics] | ||
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Latest revision as of 16:49, 22 March 2017
Journal title and website | Neurogenetics |
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Publications
Reference | Published | View | |
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Gaudo 2019 Neurogenetics | GaudΓ³ P, Emperador S, Garrido-PΓ©rez N, Ruiz-Pesini E, Yubero D, GarcΓa-Cazorla A, Artuch R, Montoya J, Bayona-Bafaluy MP (2019) Infectious stress triggers a POLG-related mitochondrial disease. Neurogenetics 21:19-27. | 2019 | PMID: 31655921 |
Isohanni 2018 Neurogenetics | Isohanni P, Carroll CJ, Jackson CB, Pohjanpelto M, LΓΆnnqvist T, Suomalainen A (2018) Defective mitochondrial ATPase due to rare mtDNA m.8969G>A mutation-causing lactic acidosis, intellectual disability, and poor growth. Neurogenetics 19:49-53. | 2018 | PMID: 29350304 |
Guillet 2010 neurogenetics | Guillet V, Gueguen N, Verny C, Ferre M, Homedan C, Loiseau D, Procaccio V, Amati-Bonneau P, Bonneau D, Reynier P, Chevrollier A (2010) Adenine nucleotide translocase is involved in a mitochondrial coupling defect in MFN2-related Charcot-Marie-Tooth type 2A disease. Neurogenetics 11:127-33. | 2010 | PMID: 19618221 |
Guillet 2010 Neurogenetics | Guillet V, Gueguen N, Verny C, Ferre M, Homedan C, Loiseau D, Procaccio V, Amati-Bonneau P, Bonneau D, Reynier P, Chevrollier A (2010) Adenine nucleotide translocase is involved in a mitochondrial coupling defect in MFN2-related Charcot-Marie-Tooth type 2A disease. Neurogenetics 11:127-33. | 2010 | PMID: 19618221 |
Cassereau 2009 Neurogenetics | Cassereau J, Chevrollier A, Gueguen N, Malinge MC, Letournel F, Nicolas G, Richard L, Ferre M, Verny C, Dubas F, Procaccio V, Amati-Bonneau P, Bonneau D, Reynier P (2009) Mitochondrial Complex I deficiency in GDAP1-related autosomal dominant Charcot-Marie-Tooth disease (CMT2K). Neurogenetics 10:145-50. | 2009 | PMID: 19089472 |