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Autor:
A D Djulepa, S Penava, S Korac, T. Frankic, H Boloban, A Bajraktarevic, J Musabegovic, A J Causevic, D Abduzaimovic, Amina Selimovic
Publikováno v:
Pediatric Research. 68:405-405
Background: Mutations in the LPL gene cause familial lipoprotein lipase deficiency. Symptoms of familial LPL deficiency usually begin in childhood and include abdominal pain, acute and recurrent inflammation of the pancreas, skin lesions called erupt