Congenital leptin deficiency due to homozygosity for the Delta133G mutation: report of another case and evaluation of response to four years of leptin therapy (Q34357127)

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Congenital leptin deficiency due to homozygosity for the Delta133G mutation: report of another case and evaluation of response to four years of leptin therapy
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    Congenital leptin deficiency due to homozygosity for the Delta133G mutation: report of another case and evaluation of response to four years of leptin therapy (English)
    Mary Moreau
    Alex M DePaoli
    Elizabeth Lawrence
    Rebecca A Trussell
    1 October 2004
    4821-4826

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