Investigation of VSX1 sequence variants in South Indian patients with sporadic cases of keratoconus
- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1756-0500
- Umfang
-
Online-Ressource
- Sprache
-
Englisch
- Anmerkungen
-
online resource.
- Erschienen in
-
Investigation of VSX1 sequence variants in South Indian patients with sporadic cases of keratoconus ; volume:6 ; number:1 ; day:18 ; month:3 ; year:2013 ; pages:1-5 ; date:12.2013
BMC Research Notes / Biomed Central; 6, Heft 1 (18.3.2013), 1-5, 12.2013
- Urheber
-
Verma, Anshuman
Das, Manoranjan
Srinivasan, Muthiah
Prajna, Namperumalsamy V.
Sundaresan, Periasamy
- Beteiligte Personen und Organisationen
-
SpringerLink (Online service)
- DOI
-
10.1186/1756-0500-6-103
- URN
-
urn:nbn:de:101:1-2021081422043157876992
- Rechteinformation
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
14.08.2025, 10:55 MESZ
Datenpartner
Dieses Objekt wird bereitgestellt von:
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Beteiligte
- Verma, Anshuman
- Das, Manoranjan
- Srinivasan, Muthiah
- Prajna, Namperumalsamy V.
- Sundaresan, Periasamy
- SpringerLink (Online service)
Ähnliche Objekte (12)
Analysis of the VSX1 gene in sporadic keratoconus patients from China
Identification of genetic variants in two families with Keratoconus
Keratoconus International Consortium (KIC)- advancing keratoconus research
USH2A gene variants cause Keratoconus and Usher syndrome phenotypes in Pakistani families
Whole exome sequencing highlights variants in association with Keratoconus in Jordanian families
Keratoconus Treatment Algorithm
Case-control association between CCT-associated variants and keratoconus in a Saudi Arabian population
Sequential sporadic-E layers at low latitudes in the Indian sector
Prediction of functional effects for sequence variants
Discordant Keratoconus in Monozygotic Twins
Ueber den Keratoconus : (Inaug. Diss.)
Sporadic Parkinsonism
Analysis of the VSX1 gene in sporadic keratoconus patients from China
Identification of genetic variants in two families with Keratoconus
Keratoconus International Consortium (KIC)- advancing keratoconus research
USH2A gene variants cause Keratoconus and Usher syndrome phenotypes in Pakistani families
Whole exome sequencing highlights variants in association with Keratoconus in Jordanian families
Keratoconus Treatment Algorithm
Case-control association between CCT-associated variants and keratoconus in a Saudi Arabian population
Sequential sporadic-E layers at low latitudes in the Indian sector
Prediction of functional effects for sequence variants
Discordant Keratoconus in Monozygotic Twins
Ueber den Keratoconus : (Inaug. Diss.)
Sporadic Parkinsonism
Analysis of the VSX1 gene in sporadic keratoconus patients from China
Identification of genetic variants in two families with Keratoconus
Keratoconus International Consortium (KIC)- advancing keratoconus research
USH2A gene variants cause Keratoconus and Usher syndrome phenotypes in Pakistani families
Whole exome sequencing highlights variants in association with Keratoconus in Jordanian families
Keratoconus Treatment Algorithm
Case-control association between CCT-associated variants and keratoconus in a Saudi Arabian population
Sequential sporadic-E layers at low latitudes in the Indian sector
Prediction of functional effects for sequence variants
Discordant Keratoconus in Monozygotic Twins
Ueber den Keratoconus : (Inaug. Diss.)