Pages that link to "Q41926642"
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The following pages link to Recognizable inherited syndrome of progressive central nervous system degeneration and generalized intracranial calcification with overlapping phenotype of the syndrome of Aicardi and Gouti�res (Q41926642):
Displaying 11 items.
- Aicardi-Goutières syndrome displays genetic heterogeneity with one locus (AGS1) on chromosome 3p21. (Q24538729) (← links)
- Structural and functional neuropathology in transgenic mice with CNS expression of IFN-alpha (Q33711550) (← links)
- Mutations in genes encoding ribonuclease H2 subunits cause Aicardi-Goutières syndrome and mimic congenital viral brain infection (Q34548112) (← links)
- Aicardi-Goutieres syndrome. (Q34917298) (← links)
- Aicardi-Goutières syndrome: monogenic recessive disease, genetically heterogeneous disease, or multifactorial disease? (Q41925364) (← links)
- Interferon-α and the calcifying microangiopathy in Aicardi-Goutières syndrome. (Q42072565) (← links)
- Aicardi-Goutieres syndrome: an oft unrecognised familial early-onset encephalopathy (Q46517025) (← links)
- Epilepsy and intracranial calcification of unknown origin. (Q48933585) (← links)
- Clinical and pathologic features of Aicardi-Goutières syndrome due to an IFIH1 mutation: A pediatric case report. (Q54217742) (← links)
- On the inheritance of "new" syndromes (Q74806044) (← links)
- Aicardi-Goutières syndrome with emphasis on sonographic features in infancy (Q84230572) (← links)