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Screening of 31 genes involved in monogenic forms of obesity in 23 Pakistani probands with early-onset childhood obesity: a case report

BACKGROUND: Consanguine families display a high degree of homozygosity which increases the risk of family members suffering from autosomal recessive disorders. Thus, homozygous mutations in monogenic obesity genes may be a more frequent cause of childhood obesity in a consanguineous population. METH...

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Detalhes bibliográficos
Publicado no:BMC Med Genet
Main Authors: Niazi, Robina Khan, Gjesing, Anette Prior, Hollensted, Mette, Have, Christian Theil, Borisevich, Dmitrii, Grarup, Niels, Pedersen, Oluf, Ullah, Asmat, Shahid, Gulbin, Shafqat, Ifrah, Gul, Asma, Hansen, Torben
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2019
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6727494/
https://ncbi.nlm.nih.gov/pubmed/31488071
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12881-019-0886-8
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