A founder mutation in TCTN2 causes Meckel‐Gruber syndrome type 8 among Jews of Ethiopian and Yemenite origin. Issue 5 (15th February 2021)

Record Type:: Journal Article
Title:: A founder mutation in TCTN2 causes Meckel‐Gruber syndrome type 8 among Jews of Ethiopian and Yemenite origin. Issue 5 (15th February 2021)
Main Title:: A founder mutation in TCTN2 causes Meckel‐Gruber syndrome type 8 among Jews of Ethiopian and Yemenite origin
Authors:: Litz Philipsborn, Shira
Hartmajer, Shulamit
Shtorch Asor, Atalia
Vinovezky, Mika
Regev, Miriam
Singer, Amihood
Reinstein, Eyal
Abstract:
Is Part Of:: American journal of medical genetics. Volume 185:Issue 5(2021)
Journal:: American journal of medical genetics
Issue:: Volume 185:Issue 5(2021)
Issue Display:: Volume 185, Issue 5 (2021)
Year:: 2021
Volume:: 185
Issue:: 5
Issue Sort Value:: 2021-0185-0005-0000
Page Start:: 1610
Page End:: 1613
Publication Date:: 2021-02-15
Subjects:: Medical genetics -- Periodicals
616.14205
Journal URLs:: http://onlinelibrary.wiley.com/ ↗
DOI:: 10.1002/ajmg.a.62119 ↗
Languages:: English
ISSNs:: 1552-4825
Deposit Type:: Legaldeposit
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗
Physical Locations:: British Library DSC - 0827.920000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store
Ingest File:: 16642.xml