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A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and In Utero Electroporation in Rodents to Identify Causative Genes for Brain Malformations
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Two patients with 'Dropped head syndrome' due to mutations in LMNA or SEPN1 genes

A D'Amico1, G Haliloglu, P Richard

  • 1Unit of Molecular Medicine, Department of Laboratory Medicine, Bambino Gesu' Children's Research Hospital, Rome, Italy.

Neuromuscular Disorders : NMD
|June 18, 2005
PubMed

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