A peroxisomal disorder of severe intellectual disability, epilepsy, and cataracts due to fatty acyl-CoA reductase 1 deficiency.
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A. Ekici | R. Abou Jamra | F. Bernier | A. Innes | H. Sticht | J. Parboosingh | R. Buchert | R. Jamra | S. Uebe | R. Lamont | B. Schwarze | Hasan Tawamie | Christopher Smith | Bassam Al Hallak | Francois P. Bernier | A. M. Innes | Bassam Al Hallak