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LRRK2 G2385R and R1628P Mutations Are Associated with an Increased Risk of Parkinson's Disease in the Malaysian Population.
- Published in:
- BioMed Research International, 2014, v. 2014, p. 1, doi. 10.1155/2014/867321
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- Article
Linkage analysis and whole exome sequencing reveals AHNAK2 as a novel genetic cause for autosomal recessive CMT in a Malaysian family.
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- Neurogenetics, 2019, v. 20, n. 3, p. 117, doi. 10.1007/s10048-019-00576-3
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- Article
Analysis of dynein intermediate chains, light intermediate chains and light chains in a cohort of hereditary peripheral neuropathies.
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- Neurogenetics, 2014, v. 15, n. 4, p. 229, doi. 10.1007/s10048-014-0414-0
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- Article
Differential diagnosis of vacuolar myopathies in the NGS era.
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- Brain Pathology, 2020, v. 30, n. 5, p. 877, doi. 10.1111/bpa.12864
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- Article
X-linked Charcot-Marie-Tooth disease predominates in a cohort of multiethnic Malaysian patients.
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- Muscle & Nerve, 2014, v. 49, n. 2, p. 198, doi. 10.1002/mus.23892
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- Article
Improved inherited peripheral neuropathy genetic diagnosis by whole-exome sequencing.
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- Molecular Genetics & Genomic Medicine, 2015, v. 3, n. 2, p. 143, doi. 10.1002/mgg3.126
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- Article