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Stability of the m.8993T→G mtDNA mutation load during human embryofetal development has implications for the feasibility of prenatal diagnosis in NARP syndrome
  1. Correspondence to:
 J Steffann
 service de génétique médicale, Hôpital Necker-Enfants Malades, 149 rue de Sèvres, 75743 Paris cedex 15, France; steffann{at}necker.fr
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Citation

Steffann J, Gigarel N, Corcos J, et al
Stability of the m.8993T→G mtDNA mutation load during human embryofetal development has implications for the feasibility of prenatal diagnosis in NARP syndrome

Publication history

  • Received December 21, 2006
  • Accepted May 11, 2007
  • Revised May 9, 2007
  • First published June 1, 2007.
Online issue publication 
October 02, 2007

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