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GM 2 gangliosidosis with hexosaminidase A and B defect: Report of a family with motor neuron disease‐like phenotype
Author(s) -
Federico A.,
Ciacci G.,
d'Amore I.,
Pallini R.,
Palmeri S.,
Rossi A.,
Rizzuto N.,
Guazzi G. C.
Publication year - 1986
Publication title -
journal of inherited metabolic disease
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.462
H-Index - 102
eISSN - 1573-2665
pISSN - 0141-8955
DOI - 10.1007/bf01799737
Subject(s) - studio , humanities , medicine , art , visual arts