A novel dominant COL11A1 mutation in a child with Stickler syndrome type II is associated with recurrent fractures

Author:

Vogiatzi M. G.,Li D.,Tian L.,Garifallou J. P.,Kim C. E.,Hakonarson H.,Levine M. A.

Funder

National Institute of Diabetes and Digestive and Kidney Diseases

Adele and Daniel Kubert Donation

National Human Genome Research Institute

Publisher

Springer Science and Business Media LLC

Subject

Endocrinology, Diabetes and Metabolism

Reference22 articles.

1. Robin NH, Moran RT, Ala-Kokko L (2000) Stickler syndrome. In: Pagon RA, Adam MP, Ardinger HH, Wallace SE, Amemiya A, Bean LJH, Bird TD, Fong CT, Mefford HC, Smith RJH, Stephens K, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2017. Jun 09 [updated March 16, 2017]

2. Acke FR, Malfait F, Vanakker OM, Steyaert W, De Leeneer K, Mortier G, Dhooge I, De Paepe A, De Leenheer EM, Coucke PJ (2014) Novel pathogenic COL11A1/COL11A2 variants in Stickler syndrome detected by targeted NGS and exome sequencing. Mol Genet Metab 113(3):230–235

3. Wang X, Jia X, Xiao X, Li S, Li J, Li Y, Wei Y, Liang X, Guo X (2016) Mutation survey and genotype-phenotype analysis of COL2A1 and COL11A1 genes in 16 Chinese patients with Stickler syndrome. Mol Vis 23(22):697–704

4. Kohmoto T, Naruto T, Kobayashi H, Watanabe M, Okamoto N, Masuda K, Imoto I, Okamoto N (2015) A novel COL11A1 mutation affecting splicing in a patient with Stickler syndrome. Hum Genome Var 12(2):15043. https://doi.org/10.1038/hgv.2015.43

5. Lara-Castillo N, Johnson ML (2015) LRP receptor family member associated bone disease. Rev Endocr Metab Disord 16(2):141–148 Review

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