Wallot, M <br/><br/>
Congenital alveolar proteinosis caused by a novel mutation of the surfactant protein B gene and misalignment of lung vessels in consanguineous kindred infants.  [electronic resource] 

 -  European journal of pediatrics  Jun 1999 
 - 513-8 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>0340-6199 
<br/><br/><label>Standard No.: </label>10.1007/s004310051132  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Blood Vessels--abnormalities<br/>Consanguinity<br/>Fatal Outcome<br/>Female<br/>Humans<br/>Infant, Newborn<br/>Lung--abnormalities<br/>Male<br/>Mutation<br/>Pedigree<br/>Polymerase Chain Reaction<br/>Proteolipids--genetics<br/>Pulmonary Alveoli--metabolism<br/>Pulmonary Surfactants--genetics