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Volumn 97, Issue 4, 2015, Pages 621-626

Loss-of-Function Mutations in the WNT Co-receptor LRP6 Cause Autosomal-Dominant Oligodontia

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CELLULAR DISTRIBUTION; CLINICAL ARTICLE; EXOME; FAMILY HISTORY; FEMALE; GENE; GENE MUTATION; GENE SEQUENCE; GENETIC VARIABILITY; GLYCOSYLATION; HETEROZYGOTE; HUMAN; HYPODONTIA; LOSS OF FUNCTION MUTATION; LOW DENSITY LIPOPROTEIN RECEPTOR RELATED PROTEIN 6 GENE; MALE; MISSENSE MUTATION; NONSENSE MUTATION; OLIGODONTIA; PRIORITY JOURNAL; PROTEIN LOCALIZATION; WNT SIGNALING PATHWAY; WNT10A GENE; CASE CONTROL STUDY; DOMINANT GENE; GENETICS; HEK293 CELL LINE; MUTATION; PATHOLOGY; PEDIGREE; PHENOTYPE;

EID: 84952720434     PISSN: 00029297     EISSN: 15376605     Source Type: Journal    
DOI: 10.1016/j.ajhg.2015.08.014     Document Type: Article
Times cited : (93)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.