LDLRAD2 c.511+7T>G

Variant ID: 1-22141323-T-G

NM_001013693.2(LDLRAD2):c.511+7T>G

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Feeding difficulty is the dominant feature in 12 Chinese newborns with CHD7 pathogenic variants.

Bmc Medical Genetics
Chen, Xiang X; Yan, Kai K; Gao, Yanyan Y; Wang, Huijun H; Chen, Guoqiang G; Wu, Bingbing B; Qin, Qian Q; Yang, Lin L; Zhou, Wenhao W
Publication Date: 2019-05-30

Variant appearance in text: LDLRAD2: 511+7T>G
PubMed Link: 31146700
Variant Present in the following documents:
  • 12881_2019_813_MOESM1_ESM.xls, sheet 1
View BVdb publication page