A Pedigree Report of a Rare Case of Weill–Marchesani Syndrome with New Compound Heterozygous LTBP2 Mutations

ZhiHong Lin,* MinJuan Zhu,* HongWei Deng Department of Strabismus & Pediatric Ophthalmology, Shenzhen Eye Hospital Affiliated to Jinan University, The School of Optometry of Shenzhen University, Shenzhen, 518000, Guangdong Province, People’s Republic of China*These authors contributed equa...

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Номзүйн дэлгэрэнгүй

Үндсэн зохиолчид:	Lin Z, Zhu M, Deng H
Формат:	Artigo
Хэл сонгох:	Inglês
Хэвлэсэн:	Dove Medical Press 2021-04-01
Цуврал:	Risk Management and Healthcare Policy
Нөхцлүүд:	weill–marchesani syndrome microspherophakia ectopia lentis ltbp2 compound heterozygous secondary glaucoma
Онлайн хандалт:	https://www.dovepress.com/a-pedigree-report-of-a-rare-case-of-weillndashmarchesani-syndrome-with-peer-reviewed-fulltext-article-RMHP
Шошгууд:	Шошго нэмэх Шошго байхгүй, Энэхүү баримтыг шошголох эхний хүн болох!