TY  - GEN
AU  - deMello,D E
AU  - Nogee,L M
AU  - Heyman,S
AU  - Krous,H F
AU  - Hussain,M
AU  - Merritt,T A
AU  - Hsueh,W
AU  - Haas,J E
AU  - Heidelberger,K
AU  - Schumacher,R
TI  - Molecular and phenotypic variability in the congenital alveolar proteinosis syndrome associated with inherited surfactant protein B deficiency
SN  - 0022-3476
PY  - 1994///0729
KW  - Female
KW  - Frameshift Mutation
KW  - Gene Expression
KW  - Genotype
KW  - Humans
KW  - Infant
KW  - Infant, Newborn
KW  - Lung
KW  - chemistry
KW  - Male
KW  - Phenotype
KW  - Proteolipids
KW  - adverse effects
KW  - Pulmonary Alveolar Proteinosis
KW  - congenital
KW  - Pulmonary Surfactant-Associated Proteins
KW  - Pulmonary Surfactants
N1  - Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S
UR  - https://doi.org/10.1016/s0022-3476(94)70119-9
ER  -