CORE
🇺🇦Â
 make metadata, not war
Services
Research
Services overview
Explore all CORE services
Access to raw data
API
Dataset
FastSync
Content discovery
Recommender
Discovery
OAI identifiers
OAI Resolver
Managing content
Dashboard
Bespoke contracts
Consultancy services
Support us
Support us
Membership
Sponsorship
Community governance
Advisory Board
Board of supporters
Research network
About
About us
Our mission
Team
Blog
FAQs
Contact us
Filters
1 research outputs found
Variant c.2158-2A>G in MANBA is an important and frequent cause of hereditary hearing loss and beta-mannosidosis among the Czech and Slovak Roma population- evidence for a new ethnic-specific variant
Author
A Broomfield
A Cooper
+46Â more
A Cooper
A Cooper
A McKenna
AH Alkhayat
Andrea Soltysova
Andrej Ficek
Anna Uhrova Meszarosova
D Gresham
D Safka Brozkova
D Safka Brozkova
D Safka Brozkova
DA Wenger
Dana Safka Brozkova
Daniela Gasperikova
E Gourrier
F Sedel
G Minarik
H Poupetova
H Wijburg
HM Riise Stensland
I Masindova
I Schrauwen
J Schwabova
J van Pelt
Jan Jencik
Jana Lastuvkova
KJ Karczewski
L Dorland
L Gort
L Kalaydjieva
L Poenaru
Lukas Varga
M Rodriguez-Serna
Martina Skopkova
MJ Landrum
P Labauge
P Lassuthova
Pavel Seeman
R Bedilu
S Bouwer
S Richards
T Levade
V Molho-Pessach
WJ Kleijer
Y Uchino
Zuzana Slobodova
Publication venue
'Springer Science and Business Media LLC'
Publication date
Field of study
No full text
Crossref
No full text
