Heterozygous LHX3 mutations may lead to a mild phenotype of combined pituitary hormone deficiency

Nicolas Jullien, Pauline Romanet, Mélanie Philippon, Marie Hélène Quentien, Paolo Beck-Peccoz, Ignacio Bergada, Sylvie Odent, Rachel Reynaud, Anne Barlier, Alexandru Saveanu, Thierry Brue, Frederic Castinetti

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Medicine & Life Sciences