Associated Papers
Mutation screening of SLC52A3, C19orf12, and TARDBP in Iranian ALS patients.
Khani M et al.
Neurobiology of Aging, 2019
Maternal riboflavin deficiency, resulting in transient neonatal-onset glutaric aciduria Type 2, is caused by a microdeletion in the riboflavin transporter gene GPR172B.
Ho G et al.
Human Mutation, 2011
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