Whole exome sequencing in an Indian family links Coats plus syndrome and dextrocardia with a homozygous novel CTC1 and a rare HES7 variation.
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| Title: | Whole exome sequencing in an Indian family links Coats plus syndrome and dextrocardia with a homozygous novel CTC1 and a rare HES7 variation. |
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| Authors: | Netravathi, Manjunath1, Kumari, Renu2, Kapoor, Saketh3, Dakle, Pushkar2, Dwivedi, Manish Kumar2, Roy, Sumitabho Deb4, Pandey, Paritosh5, Saini, Jitender6, Ramakrishna, Anil1, Navalli, Devaraddi1, Satishchandra, Parthasarathy1, Pal, Pramod Kumar1 pal.pramod@rediffmail.com, Kumar, Arun3 karun@mrdg.jisc.ernet.in, Faruq, Mohammed2 faruq.mohd@igib.res.in |
| Source: | BMC Medical Genetics. 2015, Vol. 16 Issue 1, p1-8. 8p. |
| Database: | Academic Search Ultimate |
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