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Neurofibromatosis type 2
NF2
Full NF2-related schwannomatosis
Centrum Medische Genetica - UZ Gent
Currarino syndrome
MNX1
Currarino syndrome
Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
Glycogen storage disease type 9
PHKA2
Glycogen storage disease due to liver phosphorylase kinase deficiency
Centre de Génétique Humaine - CHU Sart-Tilman
Neurodevelopmental disorders gene panel
Neurodevelopmental disorders: developmental delay, intellectual disability, autistic disorders (1162 genes) - VUB
Infantile neuroaxonal dystrophy
Centrum Medische Genetica - UZ Brussel VUB
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