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1 Ergebnisse
1
GCH1 Heterozygous Mutation Identified by Whole-Exome-Sequen..:
Fan, Zheng
;
Greenwood, Robert
;
Felix, Ana
...
Neurology. 82 (2014) 10_supplement - p. , 2014
Link:
https://doi.org/10.1212/wnl.82.10_supplement.s52.004
RT Journal T1
GCH1 Heterozygous Mutation Identified by Whole-Exome-Sequencing as a Treatable Condition in a Patient Presenting with Progressive Spastic Paraplegia (S52.004)
UL https://suche.suub.uni-bremen.de/peid=cr-10.1212_wnl.82.10_supplement.s52.004&Exemplar=1&LAN=DE A1 Fan, Zheng A1 Greenwood, Robert A1 Felix, Ana A1 Shiloh-Malawsky, Yael A1 Roche, Myra A1 Crooks, Kristy A1 Berg, Jonathan A1 Evans, James PB Ovid Technologies (Wolters Kluwer Health) YR 2014 SN 0028-3878 SN 1526-632X JF Neurology VO 82 IS 10_supplement LK http://dx.doi.org/https://doi.org/10.1212/wnl.82.10_supplement.s52.004 DO https://doi.org/10.1212/wnl.82.10_supplement.s52.004 SF ELIB - SuUB Bremen
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