Acta Neurologica Belgica

, Volume 116, Issue 4, pp 683–685 | Cite as

A case which further refines the critical region for 15q25.2 microduplication phenotypes

  • Cécile Yossa Monkam
  • Stéphan Kemeny
  • Anne Miret
  • Céline Pebrel-Richard
  • Catherine Sarret
Letter to the Editor

References

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    Wat MJ, Enciso VB, Wiszniewski et al (2010) Recurrent microdeletions of 15q25.2 are associated with increased risk of congenital diaphragmatic hernia, cognitive deficits, and possibly Diamond-Blackfan anemia. J Med Genet 47:777–781CrossRefPubMedPubMedCentralGoogle Scholar
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    Oruganty-Das A, Ng T, Udagawa T et al (2012) Translational control of mitochondrial energy production mediates neuron morphogenesis. Cell Metab 16:789–800CrossRefPubMedPubMedCentralGoogle Scholar
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    Grabner CP, Price SD, Lysakowski A et al (2006) Regulation of large dense-core vesicle volume and neurotransmitter content mediated by adaptor protein 3. Proc Natl Acad Sci USA 103:10035–10040CrossRefPubMedPubMedCentralGoogle Scholar
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Copyright information

© Belgian Neurological Society 2016

Authors and Affiliations

  • Cécile Yossa Monkam
    • 1
  • Stéphan Kemeny
    • 2
  • Anne Miret
    • 1
  • Céline Pebrel-Richard
    • 2
  • Catherine Sarret
    • 1
    • 3
  1. 1.Génétique médicaleUniversité d’Auvergne, Centre hospitalo-universitaire de Clermont-FerrandClermont-FerrandFrance
  2. 2.Cytogénétique médicaleUniversité d’Auvergne, Centre hospitalo-universitaire de Clermont-FerrandClermont-FerrandFrance
  3. 3.IGCNC, EA7282Université d’AuvergneClermont-FerrandFrance

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