Summary of mutations in ZNF644, SLC39A5, CPSF1, TNFRSF21,OPN1LWand DZIP1.

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Bibliografske podrobnosti
Glavni avtor:	Yang Liu (4829) (author)
Drugi avtorji:	Shao-Chi Zhang (22208534) (author), Wen Zhang (7555) (author), Zhong-Qi Xue (10696971) (author), Yi-Xuan Qin (22208537) (author), Shun-Yu Piao (10696963) (author), Wen-Jing Li (435085) (author), Meng-Li Ji (22208540) (author), Wen-Juan Zhuang (10696973) (author)
Izdano:	2025
Teme:	Biophysics Biochemistry Microbiology Cell Biology Genetics Molecular Biology Evolutionary Biology Developmental Biology Cancer Infectious Diseases Virology Chemical Sciences not elsewhere classified causing genes associated onset high myopia 18 candidate genes xlink "> variants xlink "> causative genes nonsyndromic myopia 18 disease znf644 </ znf644 ,</ variants observed tyr1089cys variant slc39a5 </ sanger sequencing mutation taster missense variants gnomad databases findings support exome sequencing allele frequencies 83 probands 8 %)
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Summary of mutations in <i>ZNF644, SLC39A5, CPSF1, TNFRSF21,OPN1LW</i>and <i>DZIP1.</i>