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CHD7 gene polymorphisms in female patients with idiopathic scoliosis

BACKGROUND: The CHD7 (chromosome domain helicase DNA binding protein 7) gene has been associated with familial idiopathic scoliosis (IS) in families of European descent. The CHD7 single-nucleotide polymorphisms have never been studied in Polish Caucasian IS patients. METHODS: The aim of this study w...

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Detaylı Bibliyografya
Yayımlandı:BMC Musculoskelet Disord
Asıl Yazarlar: Borysiak, Karolina, Janusz, Piotr, Andrusiewicz, Mirosław, Chmielewska, Małgorzata, Kozinoga, Mateusz, Kotwicki, Tomasz, Kotwicka, Małgorzata
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: BioMed Central 2020
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC6954548/
https://ncbi.nlm.nih.gov/pubmed/31924193
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12891-019-3031-0
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