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leptin gene mutation

Clinical significance: - rare - early-onset morbid obesity [1] - hyperphagia - hypothalamic hypogonadism - fertility generally compromised

Related

leptin receptor; LEP-R; OB receptor; OB-R; HuB219; CD295 (LEPR, DB, OBR) leptin; obesity factor; obese protein (LEP, OB, OBS) ob (leptin) receptor gene mutation

General

gene mutation testing; gene mutation analysis

References

  1. NEJM Knowledge+ Endocrinology