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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Main Authors: Chupong Ittiwut, Rungrote Natesirinilkul, Fuanglada Tongprasert, Lalita Sathitsamitphong, Chane Choed-amphai, Kanda Fanhchaksai, Pimlak Charoenkwan, Kanya Suphapeetiporn, Vorasuk Shotelersuk
Format: Journal
Published: 2018
Subjects:
Online Access: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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Institution: Chiang Mai University
id th-cmuir.6653943832-62841
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spelling 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
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
topic Medicine
spellingShingle 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
format 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
author_sort 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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