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Familial case of Blau syndrome associated with a CARD15/NOD2 mutation
by
Villanueva-Mendoza, Cristina
,
Arellanes-García, Lourdes
,
Cubas-Lorenzo, Victoria
,
Jimenez-Martinez, Maria C.
,
Flores-Suárez, Luis Felipe
,
Zenteno, Juan Carlos
Published in
Ophthalmic genetics
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Ophthalmic Genetics
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Adult
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Arthritis
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Arthritis, Rheumatoid - Genetics
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Blau
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Camptodactyly
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Card15/Nod2
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Exanthema - Genetics
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Female
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Fluorescein Angiography
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Genetics & Heredity
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Humans
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Joint Diseases - Genetics
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Life Sciences & Biomedicine
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Nod2 Signaling Adaptor Protein - Genetics
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Ophthalmology
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Pedigree
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Point Mutation
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Polymerase Chain Reaction
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Recurrence
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Taylor And Francis:jisc Collections:taylor And Francis Read And Publish Agreement 2024-2025:Medical Collection (Reading List)
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