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Summary Literature (0)
MIM:617560 - SPASTIC ATAXIA 8, AUTOSOMAL RECESSIVE, WITH HYPOMYELINATING LEUKODYSTROPHY; SPAX8

Xenbase Genes: nkx6-2

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0033043 - spastic ataxia 8, autosomal recessive, with hypomyelinating leukodystrophy