Compound SFTPB 1549C--GAA (121ins2) and 457delC heterozygosity in severe congenital lung disease and surfactant protein B (SP-B) deficiency

M Tredano; RM van Elburg; AG Kaspers; LJI Zimmermann; C Houdayer; P Aymard; WM Hull; JA Whisett; J Elion; M Griese; M Bahuau

Compound SFTPB 1549C--GAA (121ins2) and 457delC heterozygosity in severe congenital lung disease and surfactant protein B (SP-B) deficiency

M Tredano, RM van Elburg, AG Kaspers, LJI Zimmermann, C Houdayer, P Aymard, WM Hull, JA Whisett, J Elion, M Griese, M Bahuau

Pediatrics

Research output: Contribution to journal › Article › Academic › peer-review

48 Citations (Scopus)

Original language	Undefined/Unknown
Pages (from-to)	502-509
Number of pages	8
Journal	Human Mutation
Volume	14
Publication status	Published - 1999

Research programs

EMC MM-03-54-04-A

Cite this

@article{ae48ef73595b4daf9e9fc682a54c7084,

title = "Compound SFTPB 1549C--GAA (121ins2) and 457delC heterozygosity in severe congenital lung disease and surfactant protein B (SP-B) deficiency",

author = "M Tredano and {van Elburg}, RM and AG Kaspers and LJI Zimmermann and C Houdayer and P Aymard and WM Hull and JA Whisett and J Elion and M Griese and M Bahuau",

year = "1999",

language = "Undefined/Unknown",

volume = "14",

pages = "502--509",

journal = "Human Mutation",

issn = "1059-7794",

publisher = "John Wiley & Sons Inc.",

}

TY - JOUR

T1 - Compound SFTPB 1549C--GAA (121ins2) and 457delC heterozygosity in severe congenital lung disease and surfactant protein B (SP-B) deficiency

AU - Tredano, M

AU - van Elburg, RM

AU - Kaspers, AG

AU - Zimmermann, LJI

AU - Houdayer, C

AU - Aymard, P

AU - Hull, WM

AU - Whisett, JA

AU - Elion, J

AU - Griese, M

AU - Bahuau, M

PY - 1999

Y1 - 1999

M3 - Article

SN - 1059-7794

VL - 14

SP - 502

EP - 509

JO - Human Mutation

JF - Human Mutation

ER -