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Nida Fakhar
Publications
Carrier Frequency of Congenital Leptin Deficiency in Central Punjab Region of Pakistan
Congenital leptin deficiency is a rare autosomal recessive disorder, characterized by hyperphagia and early onset obesity. Worldwide data on this disorder includes only 25 cases out of this only six pathogenic mutations have been reported in the leptin gene. Most of these cases have been reported in Central Punjab region of Pakistan, harboring a (p... Read More»
Muhammad Wasim and Nida Fakhar
Research Article: J Obes Weight Loss Ther 2015, 5: 260
DOI: 10.4172/2165-7904.1000260
Abstract Peer-reviewed Full Article Peer-reviewed Article PDF
Leptin Gene Mutations in Morbidly Obese and Severely Lean Individuals from Punjab, Pakistan
Muhammad Wasim and Nida Fakhar
Research Article: J Obes Weight Loss Ther 2014, 4: 233
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