A novel mutation in intron 11 of the COL2A1 gene in a patient with type 1 Stickler syndrome.

Authors

L Leung
J C Hyland
A Young
M F Goldberg
J T Handa

Publication/Presentation Date

1-1-2006

Volume

26

Issue

1

First Page

106

Last Page

109

ISSN

0275-004X

Published In/Presented At

Leung, L., Hyland, J. C., Young, A., Goldberg, M. F., & Handa, J. T. (2006). A novel mutation in intron 11 of the COL2A1 gene in a patient with type 1 Stickler syndrome. Retina (Philadelphia, Pa.), 26(1), 106–109. https://doi.org/10.1097/00006982-200601000-00019

Disciplines

Medicine and Health Sciences

PubMedID

16395149

Department(s)

Department of Pathology and Laboratory Medicine

Document Type

Article