Clinical, biomedical , neurological and molecular study of 11 patients with new mutations in PAH gene
PKU is an autosomal recessive disorder. There is a broad spectrum phenotype which depends mainly on residual enzymatic activity and also on other factors such as modifying genes and non-genetic factors. This fact makes us consider that a multidisciplinary study of these patients is necessary to impr...
Saved in:
Published in: | Revista de neurologiá Vol. 31; no. 10; pp. 907 - 910 |
---|---|
Main Authors: | , , , , , , |
Format: | Journal Article |
Language: | Spanish |
Published: |
Spain
16-11-2000
|
Subjects: | |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Be the first to leave a comment!