- Moore, Anthony;
- Richards, AJ;
- Fincham, GS;
- McNinch, A;
- Hill, D;
- Poulson, AV;
- Castle, B;
- Lees, MM;
- Moore, AT;
- Scott, JD;
- Snead, MP
BACKGROUND: Stickler syndromes types 1, 2 and 3 are usually dominant disorders caused by mutations in the genes COL2A1, COL11A1 and COL11A2 that encode the fibrillar collagens types II and XI present in cartilage and vitreous. Rare recessive forms of Stick
