Homozygous intronic MITF mutation causes severe Waardenburg syndrome type 2A. (6th September 2018)

Record Type:
Journal Article
Title:
Homozygous intronic MITF mutation causes severe Waardenburg syndrome type 2A. (6th September 2018)
Main Title:
Homozygous intronic MITF mutation causes severe Waardenburg syndrome type 2A
Authors:
Rauschendorf, Marc‐Alexander
Zimmer, Andreas D.
Laut, Astrid
Demmer, Philipp
Rösler, Bernd
Happle, Rudolf
Sartori, Silvina
Fischer, Judith
Abstract:
Is Part Of:
Pigment cell & melanoma research. Volume 32:Number 1(2019)
Journal:
Pigment cell & melanoma research
Issue:
Volume 32:Number 1(2019)
Issue Display:
Volume 32, Issue 1 (2019)
Year:
2019
Volume:
32
Issue:
1
Issue Sort Value:
2019-0032-0001-0000
Page Start:
85
Page End:
91
Publication Date:
2018-09-06
Subjects:
Melanoma -- Periodicals
Chromatophores -- Periodicals
Animal pigments -- Periodicals
616.99477
Journal URLs:
http://www.blackwell-synergy.com/loi/pcmr ↗
http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1755-148X ↗
http://onlinelibrary.wiley.com/ ↗
DOI:
10.1111/pcmr.12733 ↗
Languages:
English
ISSNs:
1755-1471
Deposit Type:
Legaldeposit
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗
Physical Locations:
British Library DSC - 6500.147400
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store
Ingest File:
13017.xml