Exome sequencing identifies a novel INPPL1 mutation in opsismodysplasia View Full Text


Ontology type: schema:ScholarlyArticle      Open Access: True


Article Info

DATE

2013-06

AUTHORS

Aritoshi Iida, Nobuhiko Okamoto, Noriko Miyake, Nishimura, Satoshi Minami, Takuya Sugimoto, Mitsuko Nakashima, Yoshinori Tsurusaki, Hirotomo Saitsu, Masaaki Shiina, Kazuhiro Ogata, Shigehiko Watanabe, Hirofumi Ohashi, Naomichi Matsumoto, Shiro Ikegawa

ABSTRACT

Opsismodysplasia is an autosomal recessive skeletal disorder characterized by facial dysmorphism, micromelia, platyspondyly and retarded bone maturation. Recently, mutations in the gene encoding inositol polyphosphate phosphatase-like 1 (INPPL1) are found in several families with opsismodysplasia by a homozygosity mapping, followed by whole genome sequencing. We performed an exome sequencing in two unrelated Japanese families with opsismodysplasia and identified a novel INPPL1 mutation, c.1960_1962delGAG, in one family. The mutation is predicted to result in an in-frame deletion (p.E654del) within the central catalytic 5-phosphate domain. Our results further support that INPPL1 is the disease gene for opsismodysplasia and that opsismodysplasia has genetic heterogeneity. More... »

PAGES

391

References to SciGraph publications

Identifiers

URI

http://scigraph.springernature.com/pub.10.1038/jhg.2013.25

DOI

http://dx.doi.org/10.1038/jhg.2013.25

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1009290254

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/23552673


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