GM-1-GENERALIZED GANGLIOSIDOSIS VARIANT WITH CARDIOMEGALY

[1] Attal C, 1967, Ann Pediatr (Paris), V14, P457

[2] BABARIK A, 1974, LANCET, V2, P464

[3] BENSON PF, 1973, BIOCHEM SOC SPEC PUB, V1, P19

[4] BLIEDEN LC, 1974, AM J CARDIOL, V34, P83, DOI 10.1016/0002-9149(74)90097-6

[5] CRAIG JM, 1959, AMA J DIS CHILD, V98, P577

[6] ULTRASTRUCTURAL AND BIOCHEMICAL OBSERVATIONS ON A CASE OF SYSTEMIC LATE INFANTILE LIPIDOSIS AND ITS RELATIONSHIP TO TAY-SACHS DISEASE AND GARGOYLISM [J]. JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 1965, 24 (02) : 318 - &

[7] NEUROVISCERAL STORAGE DISEASE - ROENTGENOGRAPHIC FEATURES AND MODE OF INHERITANCE [J]. AMERICAN JOURNAL OF ROENTGENOLOGY RADIUM THERAPY AND NUCLEAR MEDICINE, 1968, 103 (01): : 149 - &

[8] HURLERS SYNDROME - DEFICIENCY OF A SPECIFIC BETA GALACTOSIDASE ISOENZYME [J]. SCIENCE, 1969, 165 (3893) : 611 - &

[9] KABACK MM, 1972, METHOD ENZYMOL, V27, P863

[10] FAMILIAL NEUROVISCERAL LIPIDOSIS [J]. AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1964, 108 (05): : 503 - &

[1] Attal C, 1967, Ann Pediatr (Paris), V14, P457

[2] BABARIK A, 1974, LANCET, V2, P464

[3] BENSON PF, 1973, BIOCHEM SOC SPEC PUB, V1, P19

[4] BLIEDEN LC, 1974, AM J CARDIOL, V34, P83, DOI 10.1016/0002-9149(74)90097-6

[5] CRAIG JM, 1959, AMA J DIS CHILD, V98, P577

[6] ULTRASTRUCTURAL AND BIOCHEMICAL OBSERVATIONS ON A CASE OF SYSTEMIC LATE INFANTILE LIPIDOSIS AND ITS RELATIONSHIP TO TAY-SACHS DISEASE AND GARGOYLISM [J]. JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 1965, 24 (02) : 318 - &

[7] NEUROVISCERAL STORAGE DISEASE - ROENTGENOGRAPHIC FEATURES AND MODE OF INHERITANCE [J]. AMERICAN JOURNAL OF ROENTGENOLOGY RADIUM THERAPY AND NUCLEAR MEDICINE, 1968, 103 (01): : 149 - &

[8] HURLERS SYNDROME - DEFICIENCY OF A SPECIFIC BETA GALACTOSIDASE ISOENZYME [J]. SCIENCE, 1969, 165 (3893) : 611 - &

[9] KABACK MM, 1972, METHOD ENZYMOL, V27, P863

[10] FAMILIAL NEUROVISCERAL LIPIDOSIS [J]. AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1964, 108 (05): : 503 - &