Novel FOXF1 mutations in sporadic and familial cases of alveolar capillary dysplasia with misaligned pulmonary veins imply a role for its DNA binding domain.
Hum Mutat
; 34(6): 801-11, 2013 Jun.
Article
in En
| MEDLINE
| ID: mdl-23505205
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Persistent Fetal Circulation Syndrome
/
Forkhead Transcription Factors
/
Protein Interaction Domains and Motifs
/
Mutation
Type of study:
Prognostic_studies
Limits:
Female
/
Humans
/
Infant
/
Male
/
Newborn
Language:
En
Journal:
Hum Mutat
Journal subject:
GENETICA MEDICA
Year:
2013
Document type:
Article
Affiliation country:
Country of publication: