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Novel truncation mutations in MYRF cause autosomal dominant high hyperopia mapped to 11p12–q13.3

Xueshan Xiao; Wenmin Sun; Jiamin Ouyang; Shiqiang Li; Xiaoyun Jia; Zhiqun Tan; J. Fielding Hejtmancik; Qingjiong Zhang
Human Genetics · Vol. 138, Issue 10 · pp. 1077-1090 · 2019
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Bibliographic Information

JournalHuman Genetics
PublisherSpringer
Publication Date2019-10-01
Publication Year2019
Volume138
Issue10
Pages1077-1090
Document TypeJournal Article
Print ISSN0340-6717
eISSN1432-1203
DOI10.1007/s00439-019-02039-z

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NARA Access Coverage1964-01-01~Current
Journal Homepagehttps://www.springer.com/journal/439
Publisher PageOpen Publisher Page
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