GLA and hyperinsulinemic hypoglycemia, familial, 4: Germain Germain DP DP Fabry’s disease (alpha-galactosidase—A deficiency): physiopathology, clinical signs, and genetic aspects Fabry’s disease (alpha-galactosidase—A deficiency): physiopathology, clinical signs, and genetic aspects J Soc Biol J Soc Biol 2002 2002 196 196 161 161 173 173 10.1051/jbio/2002196020161 10.1051/jbio/2002196020161 supplied-pmid 12360745?