Authors: LAMHONWAH AM TEIN I

Citation: Am. Lamhonwah et I. Tein, CARNITINE UPTAKE DEFECT - FRAMESHIFT MUTATIONS IN THE HUMAN PLASMALEMMAL CARNITINE TRANSPORTER GENE, Biochemical and biophysical research communications (Print), 252(2), 1998, pp. 396-401

Authors: KOLLURI R SHEHABELDIN A PEACOCKE M LAMHONWAH AM TEICHERTKULISZEWSKA K WEISMAN SM SIMINOVITCH KA

Citation: R. Kolluri et al., IDENTIFICATION OF WASP MUTATIONS IN PATIENTS WITH WISKOTT-ALDRICH SYNDROME AND ISOLATED THROMBOCYTOPENIA REVEALS ALLELIC HETEROGENEITY AT THE WAS LOCUS, Human molecular genetics, 4(7), 1995, pp. 1119-1126

Authors: WAKAMATSU N BENOIT G LAMHONWAH AM ZHANG ZX TRASLER JM TRIGGSRAINE BL GRAVEL RA

Citation: N. Wakamatsu et al., STRUCTURAL ORGANIZATION, SEQUENCE, AND EXPRESSION OF THE MOUSE HEXA GENE ENCODING THE ALPHA-SUBUNIT OF HEXOSAMINIDASE-A, Genomics, 24(1), 1994, pp. 110-119

Authors: LAMHONWAH AM LECLERC D LOYER M CLARIZIO R GRAVEL RA

Citation: Am. Lamhonwah et al., CORRECTION OF THE METABOLIC DEFECT IN PROPIONIC ACIDEMIA FIBROBLASTS BY MICROINJECTION OF A FULL-LENGTH CDNA OR RNA TRANSCRIPT ENCODING THEPROPIONYL-COA CARBOXYLASE BETA-SUBUNIT, Genomics, 19(3), 1994, pp. 500-505

Authors: GRAVEL RA AKERMAN BR LAMHONWAH AM LOYER M LEONDELRIO A ITALIANO I

Citation: Ra. Gravel et al., MUTATIONS PARTICIPATING IN INTERALLELIC COMPLEMENTATION IN PROPIONIC ACIDEMIA, American journal of human genetics, 55(1), 1994, pp. 51-58