Descripción de la deficiencia de alfa-1-antitripsina asociada al alelo PI*Q0Ourém en una niña de 2 años de edad y su estudio familiar. Un caso infrecuente / Alpha-1 Antitrypsin Deficiency Associated with the PI*Q0ourém Allele in a 2-Year-old Girl and Family Study. An Unusual Case
Arch. bronconeumol. (Ed. impr.)
; 54(4): 228-230, abr. 2018. ilus
Article
in Spanish
| IBECS
| ID: ibc-173037
Responsible library:
ES1.1
Localization: BNCS
RESUMEN
No disponible
Full text:
Available
Collection:
National databases
/
Spain
Database:
IBECS
Main subject:
Alpha 1-Antitrypsin Deficiency
/
Early Diagnosis
/
Alleles
/
Genotype
Type of study:
Diagnostic study
/
Risk factors
/
Screening study
Limits:
Child, preschool
/
Female
/
Humans
Language:
Spanish
Journal:
Arch. bronconeumol. (Ed. impr.)
Year:
2018
Document type:
Article
Institution/Affiliation country:
Estructuras Organizativas de Xestión Integrada (EOXI)/España