AAAS Gene - GeneCards | AAAS Protein | AAAS Antibody
Allgrove Syndrome in Iranian Patients and Report on a Novel Mutation in AAAS Gene | Iranian Journal of Pediatrics | Full Text
AAAS Gene - GeneCards | AAAS Protein | AAAS Antibody
AAAS Gene - GeneCards | AAAS Protein | AAAS Antibody
Clinical heterogeneity and molecular profile of triple A syndrome: a study of seven cases
Novel Mutations in a Patient with Triple A Syndrome
Gene: aaas (ENSDARG00000102274) - Summary - Danio_rerio - Ensembl genome browser 109
Triple A (Allgrove) syndrome: an unusual association with syringomyelia – topic of research paper in Clinical medicine. Download scholarly article PDF and read for free on CyberLeninka open science hub.
The 3230 genes you can't do without | Science | AAAS
AAAS on X: "Although attention has been directed to the X and Y sex #chromosomes, we do not understand how sex affects the rest of the #genome. Research published in @ScienceMagazine last
AAAS-achalasia, adrenocortical insufficiency, alacrimia (Allgrove, triple-A) Gene
Sequencing of the AAAS gene. Novel homozygous mutation: IVS7+1 G to A.... | Download Scientific Diagram
Schematic diagram of AAAS gene distribution of 66 mutations reported to... | Download Scientific Diagram
Identification of AAAS gene mutation in Allgrove syndrome: A report of three cases | Semantic Scholar
Clinical and molecular report of c.1331 + 1G > A mutation of the AAAS gene in a Moroccan family with Allgrove syndrome: a case report | BMC Pediatrics | Full Text
PDF) Mutation Spectra of the AAAS Gene in Iranian Families with Allgrove Syndrome | ziba soltani - Academia.edu
AAAS (Gene) - an overview | ScienceDirect Topics
AAAS Science Matters: CRISPR Gene Editing - YouTube
Triple-A syndrome with prominent ophthalmic features and a novel mutation in the AAAS gene: a case report. - UCL Discovery
Allgrove Syndrome in Iranian Patients and Report on a Novel Mutation in AAAS Gene | Iranian Journal of Pediatrics | Full Text
Clinical heterogeneity and molecular profile of triple A syndrome: a study of seven cases
Two novel truncating variants of the AAAS gene causative of the triple A syndrome | SpringerLink
Identification of AAAS gene mutation in Allgrove syndrome: A report of three cases
Aladin (AAAS) Antibody | Abbexa Ltd
Teen's leukemia goes into remission after experimental gene-editing therapy | Science | AAAS
Aladin (protein) - Wikipedia
AAAS Gene - GeneCards | AAAS Protein | AAAS Antibody
Triple A (Allgrove) syndrome due to AAAS gene mutation with a rare association of amyotrophy | SpringerLink
Phenotype–genotype spectrum of AAA syndrome from Western India and systematic review of literature in: Endocrine Connections Volume 6 Issue 8 (2017)
Triple-A syndrome with prominent ophthalmic features and a novel mutation in the AAASgene: a case report | BMC Ophthalmology | Full Text
