Author/Creator: Sheng, Xunlun - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Sheng, Xunlun

1. A novel stop codon mutation of TSPAN12 gene in Chinese patients with familial exudative vitreoretinopathy. (4th March 2022)

Authors:: Zou, Gang; Qi, Rui; Ma, Meijiao; Fu, Shangyi; Liang, Qingnan; Bi, Xiaojun; Wang, Chanjuan; Hu, Xuejun; Cai, Yujuan; Sheng, Xunlun
Journal:: Ophthalmic genetics
Issue:: Volume 43:Number 2(2022)
Page Start:: 210
Record Type:: Journal Article
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2. Association of Specific Genetic Polymorphisms with Age-related Macular Degeneration in a Northern Chinese Population. (September 2014)

Authors:: Zhuang, Wenjuan; Li, HuiPing; Liu, Yani; Zhao, Jingjing; Ha, Shaoping; Xiang, Wei; Bai, Xuewei; Li, Zili; Han, Ying; Sheng, Xunlun
Journal:: Ophthalmic genetics
Issue:: Volume 35:Number 3(2014:Sep.)
Page Start:: 156
Record Type:: Journal Article
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3. BEST1 novel mutation causes Bestrophinopathies in six families with distinct phenotypic diversity. Issue 1 (15th November 2022)

Authors:: Yang, Shangying; Li, Zhen; Cheng, Wanyu; Ma, Meijiao; Qi, Rui; Rui, Xue; Ren, Yinghua; Sheng, Xunlun; Rong, Weining
Journal:: Molecular genetics & genomic medicine
Issue:: Volume 11:Issue 1(2023)
Page Start:: n/a
Record Type:: Journal Article
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4. CEP78 is mutated in a distinct type of Usher syndrome. Issue 3 (14th September 2016)

Authors:: Fu, Qing; Xu, Mingchu; Chen, Xue; Sheng, Xunlun; Yuan, Zhisheng; Liu, Yani; Li, Huajin; Sun, Zixi; Li, Huiping; Yang, Lizhu; Wang, Keqing; Zhang, Fangxia; Li, Yumei; Zhao, Chen; Sui, Ruifang; Chen, Rui
Journal:: Journal of medical genetics
Issue:: Volume 54:Issue 3(2017)
Page Start:: 190
Record Type:: Journal Article
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5. Evaluating VEGFR1 genetic polymorphisms as a predisposition to AMD in a cohort from northern China. (1st October 2016)

Authors:: Xiang, Wei; Zhuang, Wenjuan; Chi, Hao; Sheng, Xunlun; Zhang, Wen; Xue, Zhongqi; Pan, Bo; Liu, Yang
Journal:: Ophthalmic genetics
Issue:: Volume 37:Number 4(2016)
Page Start:: 388
Record Type:: Journal Article
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6. Novel mutations in malonyl-CoA-acyl carrier protein transacylase provoke autosomal recessive optic neuropathy. (9th January 2020)

Authors:: Li, Huiping; Yuan, Shiqin; Minegishi, Yuriko; Suga, Akiko; Yoshitake, Kazutoshi; Sheng, Xunlun; Ye, Jianping; Smith, Stuart; Bunkoczi, Gabor; Yamamoto, Megumi; Iwata, Takeshi
Journal:: Human molecular genetics
Issue:: Volume 29:Number 3(2020)
Page Start:: 444
Record Type:: Journal Article
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7. Oliver-McFarlane Syndrome in a Chinese Boy: Retinitis Pigmentosa, Trichomegaly, Hair Anomalies and Mental Retardation. (March 2015)

Authors:: Sheng, Xunlun; Zhang, Shuang; Peter Boergen, Klaus; Li, Huiping; Liu, Yani
Journal:: Ophthalmic genetics
Issue:: Volume 36:Number 1(2015:Mar.)
Page Start:: 70
Record Type:: Journal Article
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8. Two novel PDE6C gene mutations in Chinese family with achromatopsia. (1st November 2020)

Authors:: Yuan, Shiqin; Qi, Rui; Fang, Xinhe; Wang, Xiaoguang; Zhou, Liang; Sheng, Xunlun
Journal:: Ophthalmic genetics
Issue:: Volume 41:Number 6(2020)
Page Start:: 591
Record Type:: Journal Article
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