Literature DB >> 5299590

Hereditary optic atrophies in childhood.

W Jaeger.   

Abstract

Entities:  

Mesh：

Year:  1966        PMID： 5299590

Source DB:  PubMed          Journal:  J Genet Hum        ISSN： 0021-7743


× No keyword cloud information.
  6 in total

Review 1.  Clinical features, molecular genetics, and pathophysiology of dominant optic atrophy.

Authors:  M Votruba; A T Moore; S S Bhattacharya
Journal:  J Med Genet       Date:  1998-10       Impact factor: 6.318

2.  [Genetic counseling in eye diseases (author's transl)].

Authors:  B Burow; U Theile
Journal:  Albrecht Von Graefes Arch Klin Exp Ophthalmol       Date:  1973-11-06

3.  Refinement of the OPA1 gene locus on chromosome 3q28-q29 to a region of 2-8 cM, in one Cuban pedigree with autosomal dominant optic atrophy type Kjer.

Authors:  A Lunkes; U Hartung; C Magariño; M Rodríguez; A Palmero; L Rodríguez; L Heredero; J Weissenbach; J Weber; G Auburger
Journal:  Am J Hum Genet       Date:  1995-10       Impact factor: 11.025

4.  Linkage analysis in dominant optic atrophy.

Authors:  J D Kivlin; E W Lovrien; D T Bishop; I H Maumenee
Journal:  Am J Hum Genet       Date:  1983-11       Impact factor: 11.025

5.  OPA1 expression in the normal rat retina and optic nerve.

Authors:  Won-Kyu Ju; Takumi Misaka; Yulia Kushnareva; Saya Nakagomi; Neeraj Agarwal; Yoshihiro Kubo; Stuart A Lipton; Ella Bossy-Wetzel
Journal:  J Comp Neurol       Date:  2005-07-18       Impact factor: 3.215

6.  Solving a 50 year mystery of a missing OPA1 mutation: more insights from the first family diagnosed with autosomal dominant optic atrophy.

Authors:  Nico Fuhrmann; Simone Schimpf; York Kamenisch; Beate Leo-Kottler; Christiane Alexander; Georg Auburger; Eberhart Zrenner; Bernd Wissinger; Marcel V Alavi
Journal:  Mol Neurodegener       Date:  2010-06-14       Impact factor: 14.195
  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.