2016•日本人類遺伝学会大会プログラム・抄録集Requires access

Detecting mutations in PRPH2 in 407 families with non-syndromic high myopia by exome sequencing

Bei Gao

Open publisher page 0 citations

Abstract

This record does not include an abstract. Use the full-text link above if available.

About this research paper

What this paper is about

An abstract is not available in the OpenAlex record for this paper.

Why it matters

A significance statement is not available in the OpenAlex record.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Key concepts: Exome sequencing, Genetics, Exome, Mutation, Medicine, Biology, Gene

Related papers

Back to paper searchBrowse research topicsOriginal source
Detecting mutations in PRPH2 in 407 families with non-syndromic high myopia by exome sequencing — Research Paper | ScholarLens