Novel compound heterozygous and homozygous variants of laminin subunit β3 gene underlie non‐Herlitz junctional epidermolysis bullosa in two paternal half‐brothers from Saudi Arabia. (6th July 2018)

Record Type:: Journal Article
Title:: Novel compound heterozygous and homozygous variants of laminin subunit β3 gene underlie non‐Herlitz junctional epidermolysis bullosa in two paternal half‐brothers from Saudi Arabia. (6th July 2018)
Main Title:: Novel compound heterozygous and homozygous variants of laminin subunit β3 gene underlie non‐Herlitz junctional epidermolysis bullosa in two paternal half‐brothers from Saudi Arabia
Authors:: Al‐Zahrani, Hams S.
Al‐Tala, Saeed
Mohamoud, Hussein S. A.
Al‐Shehri, Bandar A.
Al‐Fadhel, Saeed
Al‐Qurashi, Ali
Al‐Bishri, Ahmad
Al‐Aama, Jumana Y.
Kang, Changsoo
Betz, Regina C.
Jelani, Musharraf
Abstract:
Is Part Of:: Congenital anomalies. Volume 59:Number 3(2019)
Journal:: Congenital anomalies
Issue:: Volume 59:Number 3(2019)
Issue Display:: Volume 59, Issue 3 (2019)
Year:: 2019
Volume:: 59
Issue:: 3
Issue Sort Value:: 2019-0059-0003-0000
Page Start:: 99
Page End:: 101
Publication Date:: 2018-07-06
Subjects:: Abnormalities, Human -- Periodicals
616.043
Journal URLs:: http://onlinelibrary.wiley.com/ ↗
http://www.blackwell-synergy.com/loi/cga ↗
DOI:: 10.1111/cga.12294 ↗
Languages:: English
ISSNs:: 0914-3505
Deposit Type:: Legaldeposit
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗
Physical Locations:: British Library DSC - 3410.683000
British Library DSC - BLDSS-3PM
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Ingest File:: 10084.xml