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Novel mutations in the MNX1 gene in two families with Currarino syndrome and variable phenotype
Authors:Ellen Markljung  Tatjana Adamovic  Jia Cao  Hussein Naji  Sylvie Kaiser  Tomas Wester  Agneta Nordenskjöld
Affiliation:Department of Women's and Children's Health and Center for Molecular Medicine CMM02, Karolinska Institutet, SE-171 76 Stockholm, Sweden.
Abstract:
Keywords:CS, Currarino syndrome   CT, Computed Tomography   HB9, Homeobox 9   HCG, Human chorionic gonadotropin   HLXB9, Homeobox gene HB9   MNX1, Motor neuron and pancreas homeobox-1   MRI, Magnetic resonance imaging
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