Low Serum Alpha-1 Antitrypsin (AAT) in Family Members of Individuals with Autism Correlates with PiMZ Genotype

AIM: Deficiency of Alpha-1-antitrypsin (AAT) can be a genetic condition that increases the risk of developing liver, lung and possibly gastrointestinal disease. Since many autistic children also have gastrointestinal disorders, this study was designed to measure serum concentration of AAT and establ...

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Detalles Bibliográficos
Autores principales: Russo, Anthony J., Neville, Lauren, Wroge, Christine
Formato: Texto
Lenguaje:English
Publicado: Libertas Academica 2009
Materias:
Original Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2716675/
https://www.ncbi.nlm.nih.gov/pubmed/19652762

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2716675/
https://www.ncbi.nlm.nih.gov/pubmed/19652762

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