Recurrent intrauterine fetal loss due to near absence of HERG: Clinical and functional characterization of a homozygous nonsense HERG Q1070X mutation (vol 5, pg 553, 2008)

Journal article

Peer reviewed

Z. A. Bhuiyan, T. S. Momenah and Q. Gong

Heart rhythm, Vol.5(5), pp.773-773

01/05/2008

Abstract

Cardiac & Cardiovascular Systems

Cardiovascular System & Cardiology

Life Sciences & Biomedicine

Science & Technology

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Title: Recurrent intrauterine fetal loss due to near absence of HERG: Clinical and functional characterization of a homozygous nonsense HERG Q1070X mutation (vol 5, pg 553, 2008)
Creators - without role: Z. A. Bhuiyan
T. S. Momenah
Q. Gong
Publication Details: Heart rhythm, Vol.5(5), pp.773-773
Publisher: Elsevier
Number of pages: 1
Identifiers: 9913425008331
Academic Unit: Alfaisal University
Language: English
Resource Type: Journal article