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Clinical and genetic analysis ofHLXB9gene in Korean patients with Currarino syndrome

✍ Scribed by In-Suk Kim; Soo-young Oh; Suk-Joo Choi; Jong-Hwa Kim; Kwan Hyun Park; Hyun-Kyung Park; Jong-Won Kim; Chang-Seok Ki

Publisher
Nature Publishing Group
Year
2007
Tongue
English
Weight
261 KB
Volume
52
Category
Article
ISSN
1435-232X

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## Abstract Currarino syndrome (CS) is an autosomal dominant disorder of embryonic development characterized by the triad of anorectal abnormalities, partial sacral agenesis, and presacral mass. Mutations of the __HLXB9__ gene have been identified in most CS cases, but a precise genotype–phenotype

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