(Q42603086)

English

Allelic homogeneity in Avellino corneal dystrophy due to a founder effect

scientific article published on 10 November 2006

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

3 November 2017

Allelic homogeneity in Avellino corneal dystrophy due to a founder effect (English)

1 reference

Europe PubMed Central

PubMed publication ID

3 November 2017

corneal dystrophy

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

author name string

Kaoru Tsujikawa

1

1 reference

Europe PubMed Central

PubMed publication ID

3 November 2017

Motokazu Tsujikawa

2

1 reference

Europe PubMed Central

PubMed publication ID

3 November 2017

Hitoshi Watanabe

3

1 reference

Europe PubMed Central

PubMed publication ID

3 November 2017

Naoyuki Maeda

4

1 reference

Europe PubMed Central

PubMed publication ID

3 November 2017

Yoshitsugu Inoue

5

1 reference

Europe PubMed Central

PubMed publication ID

3 November 2017

Takashi Fujikado

6

1 reference

Europe PubMed Central

PubMed publication ID

3 November 2017

Yasuo Tano

7

1 reference

Europe PubMed Central

PubMed publication ID

3 November 2017

publication date

10 November 2006

1 reference

Europe PubMed Central

PubMed publication ID

3 November 2017

Journal of Human Genetics

1 reference

Europe PubMed Central

PubMed publication ID

3 November 2017

52

1 reference

Europe PubMed Central

PubMed publication ID

3 November 2017

1

1 reference

Europe PubMed Central

PubMed publication ID

3 November 2017

92-97

1 reference

Europe PubMed Central

PubMed publication ID

3 November 2017

Avellino Corneal Dystrophy

1 reference

https://api.crossref.org/works/10.1007%2FS10038-006-0083-4

21 January 2018

Severe corneal dystrophy phenotype caused by homozygous R124H keratoepithelin mutations

1 reference

https://pubmed.ncbi.nlm.nih.gov/17096061

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Kerato-epithelin mutations in four 5q31-linked corneal dystrophies

1 reference

https://pubmed.ncbi.nlm.nih.gov/17096061

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinically atypical granular corneal dystrophy with pathologic features of lattice-like amyloid deposits. A study of these families

1 reference

https://pubmed.ncbi.nlm.nih.gov/17096061

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Two patterns of opacity in corneal dystrophy caused by the homozygous BIG-H3 R124H mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/17096061

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

BIGH3 mutation spectrum in corneal dystrophies

1 reference

https://pubmed.ncbi.nlm.nih.gov/17096061

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of the gene responsible for gelatinous drop-like corneal dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/17096061

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Allelic homogeneity due to a founder mutation in Japanese patients with lattice corneal dystrophy type IIIA

1 reference

https://pubmed.ncbi.nlm.nih.gov/17096061

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rapid detection of M1S1 mutations by the protein truncation test

1 reference

https://pubmed.ncbi.nlm.nih.gov/17096061

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Phenotypic variation in combined granular-lattice (Avellino) corneal dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/17096061

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association of autosomal dominantly inherited corneal dystrophies with BIGH3 gene mutations in Japan

1 reference

https://pubmed.ncbi.nlm.nih.gov/17096061

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutation hot spots in 5q31-linked corneal dystrophies

1 reference

https://pubmed.ncbi.nlm.nih.gov/17096061

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S10038-006-0083-4

1 reference

Europe PubMed Central

PubMed publication ID

3 November 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

3 November 2017

ResearchGate publication ID

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