Expanding the Knowledge of KIF1A-Dependent Disorders to a Group of Polish Patients
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DOI: 10.3390/genes14050972
Abstract: Background: KIF1A (kinesin family member 1A)-related disorders encompass a variety of diseases. KIF1A variants are responsible for autosomal recessive and dominant spastic paraplegia 30 (SPG, OMIM610357), autosomal recessive hereditary sensory and autonomic neuropathy type 2… read more here.
Keywords: polish patients; knowledge kif1a; kif1a dependent; dependent disorders ... See more keywords