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
收藏
页码：392 / 392
页数：1
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