Connective Tissue

Disease	Protein	BMRB entry
Cataracts	P23T mutant of human gamma-D crystallin	16173
	Tudor domain containing 7	17835
Collagen Folding Diseases	Type-1 892 protein	17470
Hemophilia B	Human fibrillin-1	17334
Hughes syndrome	Beta 2 glycoprotein	16639
Lupus erythematosus	C-type lectin domain family 4 member D	18415
Marfan syndrome	Human fibrillin-1	17334