论文信息 - Does the association between TMEM98 and nanophthalmos require further confirmation?-Reply. - 字舞流文

Does the association between TMEM98 and nanophthalmos require further confirmation?-Reply.

Version of record (published version) freely available online following 12 month embargo from date of publication at the Publisher website .

J. Craig | K. Burdon | Mona S Awadalla

[1] A. Hewitt,et al. Mutation in TMEM98 in a large white kindred with autosomal dominant nanophthalmos linked to 17p12-q12. , 2014, JAMA ophthalmology.

[2] Chang Xian Li,et al. Identification of Transmembrane Protein 98 as a Novel Chemoresistance-Conferring Gene in Hepatocellular Carcinoma , 2014, Molecular Cancer Therapeutics.

[3] P. Söderkvist,et al. Posterior microphthalmia and nanophthalmia in Tunisia caused by a founder c.1059_1066insC mutation of the PRSS56 gene. , 2013, Gene.

[4] Chuong B. Do,et al. Genome-Wide Analysis Points to Roles for Extracellular Matrix Remodeling, the Visual Cycle, and Neuronal Development in Myopia , 2012, PLoS genetics.

[5] P. Mitchell,et al. Role of the hepatocyte growth factor gene in refractive error. , 2010, Ophthalmology.

[6] I. Bhutto,et al. Developmental Basis of Nanophthalmos: MFRP Is Required for both Prenatal Ocular Growth and Postnatal Emmetropization , 2008, Ophthalmic genetics.

[7] K. Broman,et al. Extreme hyperopia is the result of null mutations in MFRP, which encodes a Frizzled-related protein. , 2005, Proceedings of the National Academy of Sciences of the United States of America.

[8] E. Stone,et al. Myocilin glaucoma. , 2002, Survey of ophthalmology.

[9] E. Souzeau,et al. Mutation in TMEM 98 in a Large White Kindred with Autosomal Dominant Nanophthalmos Linked to 17 p 12-q 12 , 2016 .