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Mutations in the satellite cell gene MEGF10 cause a recessive congenital myopathy with minicores.
- Published in:
- Neurogenetics, 2012, v. 13, n. 2, p. 115, doi. 10.1007/s10048-012-0315-z
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- Article
A novel locus for restless legs syndrome maps to chromosome 19p in an Irish pedigree.
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- Neurogenetics, 2012, v. 13, n. 2, p. 125, doi. 10.1007/s10048-012-0317-x
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- Article
Replication study of multiple sclerosis (MS) susceptibility alleles and correlation of DNA-variants with disease features in a cohort of Austrian MS patients.
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- Neurogenetics, 2012, v. 13, n. 2, p. 181, doi. 10.1007/s10048-012-0316-y
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- Article
Frequency of SMARCB1 mutations in familial and sporadic schwannomatosis.
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- Neurogenetics, 2012, v. 13, n. 2, p. 141, doi. 10.1007/s10048-012-0319-8
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- Article
JPH3 repeat expansions cause a progressive akinetic-rigid syndrome with severe dementia and putaminal rim in a five-generation African-American family.
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- Neurogenetics, 2012, v. 13, n. 2, p. 133, doi. 10.1007/s10048-012-0318-9
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- Article
Forkhead family transcription factor FoxO and neural differentiation.
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- Neurogenetics, 2012, v. 13, n. 2, p. 105, doi. 10.1007/s10048-012-0320-2
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- Article
Systems genetic analysis of the effects of iron deficiency in mouse brain.
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- Neurogenetics, 2012, v. 13, n. 2, p. 147, doi. 10.1007/s10048-012-0321-1
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- Article
Regulation of estrogen receptor alpha gene expression in the mouse prefrontal cortex during early postnatal development.
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- Neurogenetics, 2012, v. 13, n. 2, p. 159, doi. 10.1007/s10048-012-0323-z
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- Article
Axonal transport deficit in a KIF5A mouse model.
- Published in:
- Neurogenetics, 2012, v. 13, n. 2, p. 169, doi. 10.1007/s10048-012-0324-y
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- Article