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craniometaphyseal dysplasia
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ANKH
Autosomal dominant familial calcium pyrophosphate dihydrate deposition disease is caused by mutation in the transmembrane protein ANKH
GJA1
Connexin 43 expression on peripheral blood eosinophils: role of gap junctions in transendothelial migration
Syndromic and non-syndromic disease-linked Cx43 mutations
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Oligomerization of connexins into connexons
species not specified
one gene
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External
Genetic and Functional Analysis of Craniometaphyseal Dysplasia (CMD) (CMD)