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Fibrodysplasia ossificans progressiva: Three Indian patients with mutation in the ACVR1 gene
Anju Shukla
, Onjal Taywade
, Joshi Stephen
, Divya Gupta
, Shubha R. Phadke
*
*
Corresponding author for this work
Department of Medical Genetics, Kasturba Medical College, Manipal
Research output
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Contribution to journal
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Article
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peer-review
5
Citations (Scopus)
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Dive into the research topics of 'Fibrodysplasia ossificans progressiva: Three Indian patients with mutation in the ACVR1 gene'. Together they form a unique fingerprint.
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INIS
bones
25%
children
25%
connective tissue
25%
defects
50%
detection
25%
exons
25%
genes
100%
genetics
50%
india
100%
mutations
100%
patients
100%
surgery
25%
Medicine and Dentistry
Connective Tissue
33%
Diagnostic Error
33%
Disease
33%
Exon
33%
Genetic Disorder
66%
Ossification
33%
Ossifying Myositis
100%
Prenatal Diagnosis
33%
Surgical Technique
33%
Biochemistry, Genetics and Molecular Biology
ACVR1
100%
Exon
50%
Genetic Disorder
50%
Genetics
50%
Ossification
50%
Pharmacology, Toxicology and Pharmaceutical Science
Disease
33%
Genetic Disorder
66%
Ossifying Myositis
100%