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Reply to: Double Trouble from POLG1 and CLCN1 Variants with Intrafamilial Phenotypic Heterogeneity.

Martje G PaulySinem TuncTobias BäumerGabriele Gillessen-KaesbachAlexander Münchau
Published in: Movement disorders clinical practice (2020)
Keyphrases
  • copy number
  • single cell