Association of COL1A1 and TGFB1 Polymorphisms with Otosclerosis in a Tunisian Population

Summary Otosclerosis is a condition characterized by an abnormal bone metabolism in the otic capsule, resulting in conductive and/or sensorineural hearing loss. Otosclerosis is a common disorder in which genes play an important role. Case‐control association studies have implicated several genes in...

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Veröffentlicht in:	Annals of human genetics 2011-09, Vol.75 (5), p.598-604
Hauptverfasser:	Khalfallah, Ayda, Schrauwen, Isabelle, Mnejja, Malek, HadjKacem, Hassen, Dhouib, Leila, Mosrati, Mohamed Ali, Hakim, Bochra, Lahmar, Imed, Charfeddine, Ilhem, Driss, Nabil, Ayadi, Hammadi, Ghorbel, Abdelmonem, Van Camp, Guy, Masmoudi, Saber
Format:	Artikel
Sprache:	eng
Schlagworte:	Adult Aged Bone morphogenetic protein 2 Bone morphogenetic protein 4 Bone turnover case‐control study Collagen (type I) Collagen Type I - genetics Female Gene polymorphism genetic Hearing loss Humans Male Meta‐analysis Middle Aged otosclerosis Otosclerosis - genetics Polymorphism, Single Nucleotide Sex Single-nucleotide polymorphism Transforming Growth Factor beta1 - genetics Transforming growth factor- beta 1 Tunisia
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