Chrome Extension
WeChat Mini Program
Use on ChatGLM

A Large Family with P.arg554his Mutation in ABCD1: Clinical Features and Genotype/Phenotype Correlation in Female Carriers.

Genes(2021)

Cited 3|Views12
Key words
neurogenetics,X-linked adrenoleukodystrophy,ABCD1,next generation sequencing,diagnosis
AI Read Science
Must-Reading Tree
Example
Generate MRT to find the research sequence of this paper
Chat Paper
Summary is being generated by the instructions you defined