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. 2009 Jul 21;73(3):243-5.

doi: 10.1212/WNL.0b013e3181ae7c79.

MEIS1 p.R272H in familial restless legs syndrome

C Vilariño-Güell¹, H Chai, B H Keeling, J E Young, A Rajput, T Lynch, J O Aasly, R J Uitti, Z K Wszolek, M J Farrer, S-C Lin

Affiliations

PMID: 19620614
PMCID: PMC2715576
DOI: 10.1212/WNL.0b013e3181ae7c79

MEIS1 p.R272H in familial restless legs syndrome

C Vilariño-Güell et al. Neurology. 2009.

. 2009 Jul 21;73(3):243-5.

doi: 10.1212/WNL.0b013e3181ae7c79.

Authors

C Vilariño-Güell¹, H Chai, B H Keeling, J E Young, A Rajput, T Lynch, J O Aasly, R J Uitti, Z K Wszolek, M J Farrer, S-C Lin

Affiliation

¹ Division of Neurogenetics, Department of Neuroscience, Mayo Clinic College of Medicine, Jacksonville, FL 32224, USA. VilarinoGuell.Carles@mayo.edu

PMID: 19620614
PMCID: PMC2715576
DOI: 10.1212/WNL.0b013e3181ae7c79

No abstract available

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Figures

None — Figure Conservation of MEIS1 p.R272H and segregation within pedigree (A) Protein homologues were aligned using ClustalW; p.R272H position is highlighted in black, nonconserved amino acid positions are highlighted in gray. (B) Males are represented by squares, females by circles, diamonds with a number represent the number of additional sibs. A diagonal line indicates deceased subjects, filled symbols indicate affected individuals. p.R272H mutation carriers are indicated with mt beneath the symbol, noncarriers with wt.

See this image and copyright information in PMC

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References

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