Combined immunodeficiency develops with age in Immunodeficiency-centromeric instability-facial anomalies syndrome 2 (ICF2)
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Extent
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Online-Ressource
- Language
-
Englisch
- Bibliographic citation
-
In: Orphanet Journal of Rare Diseases 2014, 9:116. DOI; http://www.ojrd.com/content/9/1/116
- Keyword
-
Histologie
Cytologie
- Event
-
Veröffentlichung
- (where)
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Würzburg
- (who)
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Universität Würzburg
- (when)
-
2015
- Creator
-
Bernuth, Horst von
Ravindran, Ethiraj
Du, Hang
Froehler, Sebastian
Strehl, Karoline
Kraemer, Nadine
Issa-Jahns, Lina
Amulic, Borko
Ninnemann, Olaf
Xiao, Mei-Sheng
Eirich, Katharina
Koelsch, Uwe
Hauptmann, Kathrin
John, Rainer
Schindler, Detlev
Wahn, Volker
Chen, Wei
Kaindl, Angela M.
- URN
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urn:nbn:de:bvb:20-opus-114859
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
25.03.2025, 1:58 PM CET
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Bernuth, Horst von
- Ravindran, Ethiraj
- Du, Hang
- Froehler, Sebastian
- Strehl, Karoline
- Kraemer, Nadine
- Issa-Jahns, Lina
- Amulic, Borko
- Ninnemann, Olaf
- Xiao, Mei-Sheng
- Eirich, Katharina
- Koelsch, Uwe
- Hauptmann, Kathrin
- John, Rainer
- Schindler, Detlev
- Wahn, Volker
- Chen, Wei
- Kaindl, Angela M.
- Universität Würzburg
Time of origin
- 2015
Other Objects (12)
ZBTB24, a gene associated with human immunodeficiency-centromere instability-facial anomalies (ICF) syndrome, regulates centromeric and pericentromeric heterochromatin formation
Common Variable Immunodeficiency
Acquired immunodeficiency syndrome
Simian immunodeficiency virus
New gene defects in combined and common variable immunodeficiency
Hematopoietic stem cell transplantation for severe combined immunodeficiency (SCID)
BCL10 deficiency presenting as severe combined immunodeficiency escaping newborn screening
Combined immunodeficiency caused by a novel nonsense mutation in LCK
Charakterisierung mütterlicher T-Zellen bei Patienten mit severe combined immunodeficiency SCID
Exome Sequencing Identifies a Novel MAP3K14 Mutation in Recessive Atypical Combined Immunodeficiency
Neopterin and Human Immunodeficiency Virus Infection
Urogenitale Infektionen bei Acquired immunodeficiency syndrome
ZBTB24, a gene associated with human immunodeficiency-centromere instability-facial anomalies (ICF) syndrome, regulates centromeric and pericentromeric heterochromatin formation
Common Variable Immunodeficiency
Acquired immunodeficiency syndrome
Simian immunodeficiency virus
New gene defects in combined and common variable immunodeficiency
Hematopoietic stem cell transplantation for severe combined immunodeficiency (SCID)
BCL10 deficiency presenting as severe combined immunodeficiency escaping newborn screening
Combined immunodeficiency caused by a novel nonsense mutation in LCK
Charakterisierung mütterlicher T-Zellen bei Patienten mit severe combined immunodeficiency SCID
Exome Sequencing Identifies a Novel MAP3K14 Mutation in Recessive Atypical Combined Immunodeficiency
Neopterin and Human Immunodeficiency Virus Infection
Urogenitale Infektionen bei Acquired immunodeficiency syndrome
ZBTB24, a gene associated with human immunodeficiency-centromere instability-facial anomalies (ICF) syndrome, regulates centromeric and pericentromeric heterochromatin formation
Common Variable Immunodeficiency
Acquired immunodeficiency syndrome
Simian immunodeficiency virus
New gene defects in combined and common variable immunodeficiency
Hematopoietic stem cell transplantation for severe combined immunodeficiency (SCID)
BCL10 deficiency presenting as severe combined immunodeficiency escaping newborn screening
Combined immunodeficiency caused by a novel nonsense mutation in LCK
Charakterisierung mütterlicher T-Zellen bei Patienten mit severe combined immunodeficiency SCID
Exome Sequencing Identifies a Novel MAP3K14 Mutation in Recessive Atypical Combined Immunodeficiency
Neopterin and Human Immunodeficiency Virus Infection