Linkage of Polymorphic Congenital Cataract to the γ-Crystallin Gene Locus on Human Chromosome 2q33–35

By Rogaev Evgeny I.   Rogaeva Ekaterina A.   Korovaitseva Galina I.   Farrer Lindsay A.   Petrin Alexander N.   Keryanov Sergey A.   Turaeva Shirine   Chumakov Ilya   George-Hyslop Peter St.   Ginter Eugeny K.  

Human Molecular Genetics, Vol. 5, Iss. 5, 1996-01 ,pp. : 699-703

Oxford University Press

Access to resources Recommend Favorite

Characterization of the G91del CRYBA1/3-crystallin protein: a cause of human inherited cataract

By Reddy M.A.   Bateman O.A.   Chakarova C.   Ferris J.   Berry V.   Lomas E.   Sarra R.   Smith M.A.   Moore A.T.   Bhattacharya S.S.   Slingsby C.  

Human Molecular Genetics, Vol. 13, Iss. 9, 2004-05 ,pp. : 945-953

Oxford University Press

Access to resources Recommend Favorite

A 5-base insertion in the γC-crystallin gene is associated with autosomal dominant variable zonular pulverulent cataract

By Ren Zhaoxia   Li Anren   Shastry Barker S.   Padma Tirunilai   Ayyagari Radha   Scott Mark H.   Parks Marshall M.   Kaiser-Kupfer Muriel I.   Hejtmancik J. Fielding  

Human Genetics, Vol. 106, Iss. 5, 2000-05 ,pp. : 531-537

Springer Publishing Company

Access to resources Recommend Favorite

Novel Mutations in the Crystallin Gene in Age-Related Cataract Patients from a North Indian Population

By  

Molecular Syndromology, Vol. 8, Iss. 4, 2017-04 ,pp. : 179-186

Karger

Access to resources Recommend Favorite

Autosomal Dominant Cerulean Cataract Is Associated with a Chain Termination Mutation in the Human β-Crystallin Gene CRYBB2

By Litt Michael  

Human Molecular Genetics, Vol. 6, Iss. 5, 1997-01 ,pp. : 665-668

Oxford University Press

Access to resources Recommend Favorite