Effect of a common missense variant in LIPA gene on fatty liver disease and lipid phenotype: New perspectives from a single‐center observational study

Abstract Lysosomal acid lipase deficiency (LAL‐D) is an autosomal recessive disease characterized by hypoalphalipoproteinemia, mixed hyperlipemia, and fatty liver (FL) due to mutations in LIPAse A, lysosomal acid type (LIPA) gene. The rs1051338 single‐nucleotide polymorphism (SNP) in LIPA gene, in v...

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Ngā taipitopito rārangi puna kōrero

Ngā kaituhi matua:	Andrea Pasta, Paolo Borro, Anna Laura Cremonini, Elena Formisano, Giulia Tozzi, Stefano Cecchi, Raffaele Fresa, Sara Labanca, Afscin Djahandideh, Samir Giuseppe Sukkar, Antonino Picciotto, Livia Pisciotta
Hōputu:	Artigo
Reo:	Inglês
I whakaputaina:	Wiley 2021-10-01
Rangatū:	Pharmacology Research & Perspectives
Ngā marau:	controlled attenuation parameter hepatic steatosis LIPA gene NAFLD rs1051338
Urunga tuihono:	https://doi.org/10.1002/prp2.820
Ngā Tūtohu:	Tāpirihia he Tūtohu Kāore He Tūtohu, Me noho koe te mea tuatahi ki te tūtohu i tēnei pūkete!