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Mutations in SNX14 Cause a Distinctive Autosomal-Recessive ..:
Thomas, Anna C
;
Williams, Hywel
;
Setó-Salvia, Núria
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4225633/. , 2014
Link:
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4225633/
RT Journal T1
Mutations in SNX14 Cause a Distinctive Autosomal-Recessive Cerebellar Ataxia and Intellectual Disability Syndrome
UL https://suche.suub.uni-bremen.de/peid=base-ftpubmed:oai:pubmedcentral.nih.gov:4225633&Exemplar=1&LAN=DE A1 Thomas, Anna C A1 Williams, Hywel A1 Setó-Salvia, Núria A1 Bacchelli, Chiara A1 Jenkins, Dagan A1 O'Sullivan, Mary A1 Mengrelis, Konstantinos A1 Ishida, Miho A1 Ocaka, Louise A1 Chanudet, Estelle A1 James, Chela A1 Lescai, Francesco A1 Anderson, Glenn A1 Morrogh, Deborah A1 Ryten, Mina A1 Duncan, Andrew J A1 Pai, Yun Jin A1 Saraiva, Jorge M A1 Ramos, Fabiana A1 Farren, Bernadette A1 Saunders, Dawn A1 Vernay, Bertrand A1 Gissen, Paul A1 Straatmaan-Iwanowska, Anna A1 Baas, Frank A1 Wood, Nicholas W A1 Hersheson, Joshua A1 Houlden, Henry A1 Hurst, Jane A1 Scott, Richard A1 Bitner-Glindzicz, Maria A1 Moore, Gudrun E A1 Sousa, Sérgio B A1 Stanier, Philip PB Elsevier YR 2014 K1 Report JF http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4225633/ LK http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4225633/ DO http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4225633/ SF ELIB - SuUB Bremen
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