Whole-exome sequencing for the genetic diagnosis of congenital red blood cell membrane disorders in Taiwan-Reference-Cited by-同舟云学术

Whole-exome sequencing for the genetic diagnosis of congenital red blood cell membrane disorders in Taiwan

Published:2018-12 Issue: Volume:487 Page:311-317
ISSN:0009-8981
Container-title:Clinica Chimica Acta
language:en
Short-container-title:Clinica Chimica Acta

Author:

Lin Pei-Chin,Chiou Shyh-Shin,Lin Chien-Yu,Wang Shu-Chen,Huang Hsi-Yuan,Chang Ya-Sian,Tseng Yu-Hsin,Kan Tzu-Min,Liao Yu-Mei,Tsai Shih-Pien,Peng Ching-Tien,Chang Jan-Gowth^ORCID

Funder

Ministry of Science and Technology

Kaohsiung Medical University Hospital

Publisher

Elsevier BV

Subject

Biochemistry (medical),Clinical Biochemistry,Biochemistry,General Medicine

Reference36 articles.

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4. Spectrin Tunis (Sp alpha (I/78)) in a Korean family with hereditary elliptocytosis;Han;Ann Lab Med,2013

5. Mutational characteristics of ANK1 and SPTB genes in hereditary spherocytosis;Park;Clin. Genet.,2016

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