Correction: Mutations in the homeodomain of HOXD13 cause syndactyly type 1-c in two Chinese families (PLoS ONE (2014) 9, 5 (e96192) DOI: 10.1371/journal.pone.0096192);Mutations in the homeodomain of HOXD13 cause syndactyly type 1-c in two Chinese families

PLoS ONE

Volumn 9, Issue 5, 2014, Pages

  Dai, Limeng ^a   Liu, Dan ^a   Song, Min ^a   Xu, Xueqing ^a   Xiong, Gang ^a   Yang, Kang ^a   Zhang, Kun ^a   Meng, Hui ^a   Guo, Hong ^a   Bai, Yun ^a  

^a THIRD MILITARY MEDICAL UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

HOMEODOMAIN PROTEIN; HOXD13 PROTEIN, HUMAN; TRANSCRIPTION FACTOR;

ARTICLE; BINDING AFFINITY; CHINESE; COMPARATIVE GENOMIC HYBRIDIZATION; CONTROLLED STUDY; COPY NUMBER VARIATION; DISEASE ASSOCIATION; FEMALE; GENE; GENE DELETION; GENE DUPLICATION; GENE IDENTIFICATION; GENE MAPPING; GENE SEQUENCE; GENETIC ASSOCIATION; GENETIC VARIABILITY; GENOTYPE; HOXD13 GENE; HUMAN; LIMB DEVELOPMENT; MAJOR CLINICAL STUDY; MALE; MISSENSE MUTATION; NUCLEOTIDE SEQUENCE; OVERLAPPING GENE; PATHOGENESIS; PHENOTYPE; SEQUENCE ANALYSIS; SYNDACTYLY; SYNDACTYLY TYPE 1; ASIAN CONTINENTAL ANCESTRY GROUP; CHINA; CHROMOSOME 2; GENETIC LINKAGE; GENETICS; PATHOLOGY; PEDIGREE;

ASIAN CONTINENTAL ANCESTRY GROUP; CHINA; CHROMOSOMES, HUMAN, PAIR 2; FEMALE; GENETIC LINKAGE; HOMEODOMAIN PROTEINS; HUMANS; MALE; MUTATION, MISSENSE; PEDIGREE; PHENOTYPE; SYNDACTYLY; TRANSCRIPTION FACTORS;

EID: 84900320600     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0104309     Document Type: Erratum

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