Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C T (Arg493X) mutation: an international initiative

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DOIResolve DOI: https://doi.org/10.1016/S1474-4422(07)70221-1
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NRC number1773
NPARC number3538364
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Record created2009-03-01
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