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Homozygous deletion of glutamate receptor gene GRID2 causes early-onset cerebellar ataxia and retinal dystrophy
Homozygous deletion of glutamate receptor gene GRID2 causes early-onset cerebellar ataxia and retinal dystrophy
2014
Kristof Van Schil
Marcus Karlstetter
Françoise Meire
Miriam Bauwens
Hannah Verdin
Frauke Coppieters
Eva Scheiffert
Nicolas Deconinck
Thomas Langmann
Elfride De Baere
Keywords:
Early Onset Cerebellar Ataxia
Retinal
Gene
Endocrinology
Glutamate receptor
Dystrophy
GRID2
Medicine
Internal medicine
retinal dystrophy
Correction
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