Identification of a novel deep intronic variant in CRTAP by genome sequencing as the cause of osteogenesis imperfecta

被引：0

作者：

Bhavani, Gandham SriLakshmi ^{[1
]}

Udupa, Prajna ^{[1
]}

Nayak, Shalini ^{[1
]}

Kausthubham, Neethukrishna ^{[1
]}

Dalal, Ashwin ^{[2
]}

Girisha, Katta ^{[1
]}

机构：

[1] Manipal Acad Higher Educ, Kasturba Med Coll Manipal, Manipal, India

[2] Ctr DNA Fingerprinting & Diagnost, Div Diagnost, Hyderabad, India

来源：

EUROPEAN JOURNAL OF HUMAN GENETICS | 2023年 / 31卷

关键词：

D O I：

暂无

中图分类号：

Q5 [生物化学]; Q7 [分子生物学];

学科分类号：

071010 ; 081704 ;

摘要：

P05.019.D

引用

页码：392 / 392

页数：1

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