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

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

DOI Full Paper Access

27

Citations

32

References

2018

Year

Nicolas Jullien, Pauline Romanet, Mélanie Philippon, Marie-Hélène Quentien, Paolo Beck‐Peccoz, Ignacio Bergadá, Sylvie Odent, Rachel Reynaud, Anne Barlier, Alexandru Saveanu,

European Journal of Human Genetics

Developmental BiologyPituitary GlandGrowth HormoneHuman GrowthEndocrine MechanismGeneticsHeterozygous Lhx3 MutationsReceptor BiologyPituitary DiseaseEndocrinologyMedicineMild Phenotype

References

	Year	Citations

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