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1 Ergebnisse
1
First Genotype-Phenotype Study in TBX4 Syndrome: Gain-of-Fu..:
Prapa, Matina
;
Lago-Docampo, Mauro
;
Swietlik, Emilia M
...
boreal:278235. , 2022
Link:
http://hdl.handle.net/2078.1/278235
RT Journal T1
First Genotype-Phenotype Study in TBX4 Syndrome: Gain-of-Function Mutations Causative for Lung Disease
UL https://suche.suub.uni-bremen.de/peid=base-ftunistlouisbrus:oai:dial.uclouvain.be:boreal:278235&Exemplar=1&LAN=DE A1 Prapa, Matina A1 Lago-Docampo, Mauro A1 Swietlik, Emilia M A1 Montani, David A1 Eyries, Mélanie A1 Humbert, Marc A1 Welch, Carrie L A1 Chung, Wendy K A1 Berger, Rolf M F A1 Bogaard, Harm Jan A1 Danhaive, Olivier A1 Escribano-Subías, Pilar A1 Gall, Henning A1 Girerd, Barbara A1 Hernandez-Gonzalez, Ignacio A1 Holden, Simon A1 Hunt, David A1 Jansen, Samara M A A1 Kerstjens-Frederikse, Wilhelmina A1 Kiely, David G A1 Lapunzina, Pablo A1 McDermott, John A1 Moledina, Shahin A1 Pepke-Zaba, Joanna A1 Polwarth, Gary J A1 Schotte, Gwen A1 Tenorio-Castaño, Jair A1 Thompson, A A Roger A1 Wharton, John A1 Wort, Stephen J A1 Megy, Karyn A1 Mapeta, Rutendo A1 Treacy, Carmen M A1 Martin, Jennifer M A1 Li, Wei A1 Swift, Andrew J A1 Upton, Paul D A1 Morrell, Nicholas W A1 Gräf, Stefan A1 Valverde, Diana A1 NIHR BioResource for Translational Research–Rare Diseases A1 National Cohort Study of Idiopathic and Heritable PAH A1 PAH Biobank Enrolling Centers' Investigators PB American Thoracic Society YR 2022 K1 Humans K1 Gain of Function Mutation K1 T-Box Domain Proteins K1 Bone Morphogenetic Protein Receptors K1 Type II K1 Phenotype K1 Lung Diseases K1 Mutation K1 Genotype K1 TBX4 K1 gain-of-function K1 interstitial lung disease K1 lung developmental disease K1 pulmonary arterial hypertension JF boreal:278235 LK http://hdl.handle.net/2078.1/278235 DO http://hdl.handle.net/2078.1/278235 SF ELIB - SuUB Bremen
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