Literature DB >> 11705153

Albinism.

I Russell-Eggitt1.   

Abstract

Albinism is a heterogeneous group of conditions having in common a hereditary error of melanin metabolism resulting in misrouting of optic nerve fibers during embryogenesis, underdevelopment of the neuroretinas, and in varying degrees of hypopigmentation of eyes, skin, and hair.

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Mesh:

Year:  2001        PMID: 11705153     DOI: 10.1016/s0896-1549(05)70251-0

Source DB:  PubMed          Journal:  Ophthalmol Clin North Am        ISSN: 0896-1549


  3 in total

1.  Chiasmal misrouting and foveal hypoplasia without albinism.

Authors:  M M van Genderen; F C C Riemslag; J Schuil; F P Hoeben; J S Stilma; F M Meire
Journal:  Br J Ophthalmol       Date:  2006-05-17       Impact factor: 4.638

2.  Tyrosinase is the modifier of retinoschisis in mice.

Authors:  Britt A Johnson; Brian S Cole; Eldon E Geisert; Sakae Ikeda; Akihiro Ikeda
Journal:  Genetics       Date:  2010-09-27       Impact factor: 4.562

3.  L-DOPA is an endogenous ligand for OA1.

Authors:  Vanessa M Lopez; Christina L Decatur; W Daniel Stamer; Ronald M Lynch; Brian S McKay
Journal:  PLoS Biol       Date:  2008-09-30       Impact factor: 8.029

  3 in total

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