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Literature for DOID 14177: congenital hypogammaglobulinemia
Xenbase Articles

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Multisystem disorder associated with a pathogenic variant in CLCN7 in the absence of osteopetrosis.,
Lee CL,Chang YW,Lin HY,Lee HC,Yeh TC,Fang LC,Lee NC,Tsai JD,Lin SP,
Mol Genet Genomic Med. July 1, 2024; 12(7):2324-9269.
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