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Neurogenetics|May 12, 2017
Hypomyelinating leukodystrophy associated with a deleterious mutation in the ATRN geneMaher Awni Shahrour, Motee Ashhab, Simon Edvardson, et al.
Neurogenetics|March 17, 2010
Molecular characterization of six Chinese families with m.3460G>A and Leber hereditary optic neuropathyDandan Yu, Xiaoyun Jia, A-Mei Zhang, et al.
Neurogenetics|March 12, 2009
Neuronal ceroid lipofuscinosis caused by MFSD8 mutations: a common theme emergingM A Aldahmesh, Z N Al-Hassnan, M Aldosari, et al.
Neurogenetics|March 14, 2009
Ashkenazi Parkinson's disease patients with the LRRK2 G2019S mutation share a common founder dating from the second to fifth centuriesAnat Bar-Shira, Carolyn M Hutter, Nir Giladi, et al.
Neurogenetics|March 3, 2009
Molecular analysis of NPC1 and NPC2 gene in 34 Niemann-Pick C Italian patients: identification and structural modeling of novel mutationsTatiana Fancello, Andrea Dardis, Camillo Rosano, et al.
Neurogenetics|May 28, 2009
SCA27 caused by a chromosome translocation: further delineation of the phenotypeD Misceo, M Fannemel, T Barøy, et al.
Neurogenetics|May 22, 2009
LRRK2 and GBA mutations differentially affect the initial presentation of Parkinson diseaseZ Gan-Or, A Bar-Shira, A Mirelman, et al.
Neurogenetics|October 3, 2008
Assessment of Alzheimer's disease case-control associations using family-based methodsBrit-Maren M Schjeide, Matthew B McQueen, Kristina Mullin, et al.
Neurogenetics|January 21, 2009
Familial hemiplegic migraine: linkage to chromosome 14q32 in a Spanish kindredEster Cuenca-León, Roser Corominas, Magda Montfort, et al.
Neurogenetics|September 21, 2005
Lrrk2 pathogenic substitutions in Parkinson's diseaseIgnacio F Mata, Jennifer M Kachergus, Julie P Taylor, et al.
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