A Chinese girl with fibrodysplasia ossificans progressiva caused by a de novo mutation R206H in ACVR1 gene.

Zhonghua er ke za zhi. Chinese journal of pediatrics

Volumn 46, Issue 3, 2008, Pages 215-219

  Zhou, Qing ^a   Meng, Yan ^b   Su, Liang ^b   Zhao, Shi min ^b   Shi, Hui ping ^b   Huang, Shang zhi ^b  

^a PEKING UNION MEDICAL COLLEGE   (China)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

ACTIVIN RECEPTOR 1; ACVR1 PROTEIN, HUMAN;

ARTICLE; ASIAN; CASE REPORT; DNA SEQUENCE; FEMALE; GENETICS; HUMAN; MOLECULAR GENETICS; NUCLEOTIDE SEQUENCE; OSSIFYING MYOSITIS; POINT MUTATION; PRESCHOOL CHILD;

ACTIVIN RECEPTORS, TYPE I; ASIAN CONTINENTAL ANCESTRY GROUP; BASE SEQUENCE; CHILD, PRESCHOOL; FEMALE; HUMANS; MOLECULAR SEQUENCE DATA; MYOSITIS OSSIFICANS; POINT MUTATION; SEQUENCE ANALYSIS, DNA;

EID: 84863954994     PISSN: 05781310     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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