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

L. Leung, J. C. Hyland, A. Young, Morton F Goldberg, James Handa

Research output: Contribution to journalArticle

Original languageEnglish (US)
Pages (from-to)106-109
Number of pages4
JournalRetina
Volume26
Issue number1
DOIs
StatePublished - Jan 2006

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DNA Mutational Analysis
Molecular Sequence Data
Eye Abnormalities
Vitreous Body
Retinal Perforations
Collagen Type II
Myopia
Optical Coherence Tomography
Retinal Detachment
Introns
Polymerase Chain Reaction
Mutation
Genes
Type 1 Stickler syndrome

ASJC Scopus subject areas

  • Ophthalmology
  • Sensory Systems

Cite this

A novel mutation in intron 11 of the COL2A1 gene in a patient with type 1 Stickler syndrome. / Leung, L.; Hyland, J. C.; Young, A.; Goldberg, Morton F; Handa, James.

In: Retina, Vol. 26, No. 1, 01.2006, p. 106-109.

Research output: Contribution to journalArticle

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