reference/474362

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publicationName	Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration
startingPage	615
bibliographicCitation	Vengoechea J, David MP, Yaghi SR, Carpenter L, Rudnicki SA. Clinical variability and female penetrance in X-linked familial FTD/ALS caused by a P506S mutation in UBQLN2. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration. 2013 Aug 14;14(7-8):615–9. doi: 10.3109/21678421.2013.824001.
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date	2013-08-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://doi.org/10.3109/21678421.2013.824001 https://pubmed.ncbi.nlm.nih.gov/23944734
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language	English
source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	Clinical variability and female penetrance in X-linked familial FTD/ALS caused by a P506S mutation in UBQLN2
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