Publication | Open Access
Loss-of-function mutations in the melanocortin 4 receptor in a UK birth cohort
121
Citations
38
References
2021
Year
Developmental BiologyMelanocortin 4Genetic DisorderGeneticsGenetic EpidemiologyLoss-of-function MutationsUk Birth CohortMedicineEpigeneticsVariant InterpretationClinical GeneticsGenetic Medicine
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