Associated Papers
Identification of a novel genetic locus underlying tremor and dystonia.
Monies D et al.
Human Genomics, 2017
29110692 (PubMed )
Supplement: 40246_2017_123_MOESM2_ESM.pdf
TBX1 mutation identified by exome sequencing in a Japanese family with 22q11.2 deletion syndrome-like craniofacial features and hypocalcemia.
Ogata T et al.
Plos One, 2014
24637876 (PubMed )
Supplement: pone.0091598.s007.pdf
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