DOI:
10.1055/s-00000041
Neuropediatrics
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References
Haack TB, Hogarth P, Kruer MC. , et al.
Exome sequencing reveals de novo WDR45 mutations causing a phenotypically distinct, X-linked dominant form of NBIA.
Am J Hum Genet 2012;
91 (06) 1144-1149
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