First Genotype-Phenotype Study in TBX4 Syndrome Gain-of-Function Mutations Causative for Lung Disease
- Prapa, M.
- Lago-Docampo, M.
- Swietlik, E.M.
- Montani, D.
- Eyries, M.
- Humbert, M.
- Welch, C.L.
- Chung, W.K.
- Berger, R.M.F.
- Bogaard, H.J.
- Danhaive, O.
- Escribano-Subías, P.
- Gall, H.
- Girerd, B.
- Hernandez-Gonzalez, I.
- Holden, S.
- Hunt, D.
- Jansen, S.M.A.
- Kerstjens-Frederikse, W.
- Kiely, D.G.
- Lapunzina, P.
- McDermott, J.
- Moledina, S.
- Pepke-Zaba, J.
- Polwarth, G.J.
- Schotte, G.
- Tenorio-Castaño, J.
- Thompson, A.A.R.
- Wharton, J.
- Wort, S.J.
- Megy, K.
- Mapeta, R.
- Treacy, C.M.
- Martin, J.M.
- Li, W.
- Swift, A.J.
- Upton, P.D.
- Morrell, N.W.
- Gräf, S.
- Valverde, D.
- Alle Autoren anzeigen +
ISSN: 1535-4970, 1073-449X
Datum der Publikation: 2022
Ausgabe: 206
Nummer: 12
Seiten: 1522-1533
Art: Artikel