A Novel Missense Mutation in SRD5A3 Causes Congenital Disorder of Glycosylation Type I Read more about A Novel Missense Mutation in SRD5A3 Causes Congenital Disorder of Glycosylation Type I
Mutations in Zinc Finger 407 [ZNF407] cause a Unique Autosomal Recessive Cognitive Impairment Syndrome Read more about Mutations in Zinc Finger 407 [ZNF407] cause a Unique Autosomal Recessive Cognitive Impairment Syndrome
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