Clinical phenotype associated with the arg141 his mutation in the X-linked retinoschisis gene.

v1

Type:Journal Article

0 views

[![NobleID](https://www.nobleid.org/api/badge/7DA2DB67.svg?ark=w1%2F20260515%2F7DA2DB67)](https://nobleid.org/work/w1/20260515/7DA2DB67)

ARK Inflections

Bibliometric Analysis

Impact metrics, research fronts, co-authorship networks →

Authors & Claims

Paper Authors