Mysteries of α1-antitrypsin deficiency: emerging therapeutic strategies for a challenging disease
R Ghouse, A Chu, Y Wang… - Disease models & …, 2014 - journals.biologists.com
The classical form of α1-antitrypsin deficiency (ATD) is an autosomal co-dominant disorder
that affects~ 1 in 3000 live births and is an important genetic cause of lung and liver disease …
that affects~ 1 in 3000 live births and is an important genetic cause of lung and liver disease …
[HTML][HTML] Mysteries of α1-antitrypsin deficiency: emerging therapeutic strategies for a challenging disease.
R Ghouse, A Chu, Y Wang… - Disease Models & …, 2014 - europepmc.org
The classical form of α1-antitrypsin deficiency (ATD) is an autosomal co-dominant disorder
that affects~ 1 in 3000 live births and is an important genetic cause of lung and liver disease …
that affects~ 1 in 3000 live births and is an important genetic cause of lung and liver disease …
Mysteries of α1-antitrypsin deficiency: emerging therapeutic strategies for a challenging disease
R Ghouse, A Chu, Y Wang… - Disease models & …, 2014 - pubmed.ncbi.nlm.nih.gov
The classical form of α1-antitrypsin deficiency (ATD) is an autosomal co-dominant disorder
that affects~ 1 in 3000 live births and is an important genetic cause of lung and liver disease …
that affects~ 1 in 3000 live births and is an important genetic cause of lung and liver disease …
Mysteries of α1-antitrypsin deficiency: Emerging therapeutic strategies for a challenging disease
R Ghouse, A Chu, Y Wang… - DMM Disease Models …, 2014 - profiles.wustl.edu
The classical form of α1-antitrypsin deficiency (ATD) is an autosomal co-dominant disorder
that affects∼ 1 in 3000 live births and is an important genetic cause of lung and liver …
that affects∼ 1 in 3000 live births and is an important genetic cause of lung and liver …
[PDF][PDF] Mysteries of α1-antitrypsin deficiency: emerging therapeutic strategies for a challenging disease
R Ghouse, A Chu, Y Wang, DH Perlmutter - 2014 - cyberleninka.org
The classical form of α1-antitrypsin deficiency (ATD) is an autosomal co-dominant disorder
that affects~ 1 in 3000 live births and is an important genetic cause of lung and liver disease …
that affects~ 1 in 3000 live births and is an important genetic cause of lung and liver disease …
[PDF][PDF] Mysteries of α1-antitrypsin deficiency: emerging therapeutic strategies for a challenging disease
R Ghouse, A Chu, Y Wang, DH Perlmutter - 2014 - researchgate.net
The classical form of α1-antitrypsin deficiency (ATD) is an autosomal co-dominant disorder
that affects~ 1 in 3000 live births and is an important genetic cause of lung and liver disease …
that affects~ 1 in 3000 live births and is an important genetic cause of lung and liver disease …
[HTML][HTML] Mysteries of α1-antitrypsin deficiency: emerging therapeutic strategies for a challenging disease
R Ghouse, A Chu, Y Wang… - Disease Models & …, 2014 - ncbi.nlm.nih.gov
The classical form of α1-antitrypsin deficiency (ATD) is an autosomal co-dominant disorder
that affects~ 1 in 3000 live births and is an important genetic cause of lung and liver disease …
that affects~ 1 in 3000 live births and is an important genetic cause of lung and liver disease …
Mysteries of α1-antitrypsin deficiency: emerging therapeutic strategies for a challenging disease
R Ghouse, A Chu, Y Wang… - Disease Models & …, 2014 - search.proquest.com
The classical form of α1-antitrypsin deficiency (ATD) is an autosomal co-dominant disorder
that affects~ 1 in 3000 live births and is an important genetic cause of lung and liver disease …
that affects~ 1 in 3000 live births and is an important genetic cause of lung and liver disease …
Mysteries of α1-antitrypsin deficiency: emerging therapeutic strategies for a challenging disease.
R Ghouse, A Chu, Y Wang… - Disease Models & …, 2014 - europepmc.org
The classical form of α1-antitrypsin deficiency (ATD) is an autosomal co-dominant disorder
that affects~ 1 in 3000 live births and is an important genetic cause of lung and liver disease …
that affects~ 1 in 3000 live births and is an important genetic cause of lung and liver disease …