Clinical features of neurodegeneration with brain iron accumulation due to a C19orf12 gene mutation.
Goldman JG; Eichenseer SR; Berry-Kravis E; Zimnowodzki S; Gregory A; Hogarth P; Hayflick SJ; Movement Disorders: Official Journal Of The Movement Disorder Society, 2013, vol. 28, issue 10, p 1462, ISSN 15318257. ISBN 15318257.

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