Novel mutations in SPTA1 and SPTB identified by whole exome sequencing in eight Thai families with hereditary pyropoikilocytosis presenting with severe fetal and neonatal anaemia
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2018
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th-cmuir.6653943832-628412018-11-29T07:54:20Z Novel mutations in SPTA1 and SPTB identified by whole exome sequencing in eight Thai families with hereditary pyropoikilocytosis presenting with severe fetal and neonatal anaemia Chupong Ittiwut Rungrote Natesirinilkul Fuanglada Tongprasert Lalita Sathitsamitphong Chane Choed-amphai Kanda Fanhchaksai Pimlak Charoenkwan Kanya Suphapeetiporn Vorasuk Shotelersuk Medicine 2018-11-29T07:54:20Z 2018-11-29T07:54:20Z 2018-01-01 Journal 13652141 00071048 2-s2.0-85053051054 10.1111/bjh.15559 https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85053051054&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/62841 |
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Chiang Mai University |
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Chiang Mai University Library |
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Medicine |
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Medicine Chupong Ittiwut Rungrote Natesirinilkul Fuanglada Tongprasert Lalita Sathitsamitphong Chane Choed-amphai Kanda Fanhchaksai Pimlak Charoenkwan Kanya Suphapeetiporn Vorasuk Shotelersuk Novel mutations in SPTA1 and SPTB identified by whole exome sequencing in eight Thai families with hereditary pyropoikilocytosis presenting with severe fetal and neonatal anaemia |
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Journal |
author |
Chupong Ittiwut Rungrote Natesirinilkul Fuanglada Tongprasert Lalita Sathitsamitphong Chane Choed-amphai Kanda Fanhchaksai Pimlak Charoenkwan Kanya Suphapeetiporn Vorasuk Shotelersuk |
author_facet |
Chupong Ittiwut Rungrote Natesirinilkul Fuanglada Tongprasert Lalita Sathitsamitphong Chane Choed-amphai Kanda Fanhchaksai Pimlak Charoenkwan Kanya Suphapeetiporn Vorasuk Shotelersuk |
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Chupong Ittiwut |
title |
Novel mutations in SPTA1 and SPTB identified by whole exome sequencing in eight Thai families with hereditary pyropoikilocytosis presenting with severe fetal and neonatal anaemia |
title_short |
Novel mutations in SPTA1 and SPTB identified by whole exome sequencing in eight Thai families with hereditary pyropoikilocytosis presenting with severe fetal and neonatal anaemia |
title_full |
Novel mutations in SPTA1 and SPTB identified by whole exome sequencing in eight Thai families with hereditary pyropoikilocytosis presenting with severe fetal and neonatal anaemia |
title_fullStr |
Novel mutations in SPTA1 and SPTB identified by whole exome sequencing in eight Thai families with hereditary pyropoikilocytosis presenting with severe fetal and neonatal anaemia |
title_full_unstemmed |
Novel mutations in SPTA1 and SPTB identified by whole exome sequencing in eight Thai families with hereditary pyropoikilocytosis presenting with severe fetal and neonatal anaemia |
title_sort |
novel mutations in spta1 and sptb identified by whole exome sequencing in eight thai families with hereditary pyropoikilocytosis presenting with severe fetal and neonatal anaemia |
publishDate |
2018 |
url |
https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85053051054&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/62841 |
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1681425882141425664 |