(Q28281873)

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Molecular basis of an adult form of beta-hexosaminidase B deficiency with motor neuron disease

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title

Molecular basis of an adult form of beta-hexosaminidase B deficiency with motor neuron disease (English)

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1 reference

P Banerjee

1

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L Siciliano

series ordinal

2

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D Oliveri

series ordinal

3

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N R McCabe

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4

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M J Boyers

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5

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A L Horwitz

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6

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S C Li

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7

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G Dawson

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8

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language of work or name

English

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publication date

27 November 1991

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published in

Biochemical and Biophysical Research Communications

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volume

181

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issue

1

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page(s)

108-15

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cites work

Report of the committee on linkage and gene order

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https://api.crossref.org/works/10.1016%2FS0006-291X%2805%2981388-9

retrieved

7 January 2021

A new point mutation within exon 5 of beta-hexosaminidase alpha gene in a Japanese infant with Tay-Sachs disease.

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https://api.crossref.org/works/10.1016%2FS0006-291X%2805%2981388-9

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7 January 2021

N-acetyl-beta-hexosaminidase B deficiency in cultured fibroblasts from a patient with progressive motor neuron disease

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7 January 2021

N-acetyl-beta-hexosaminidase beta locus defect and juvenile motor neuron disease: a case study

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7 January 2021

Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase

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7 January 2021

A new variant of Type-AB GM2-gangliosidosis

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7 January 2021

Influence of interior packing and hydrophobicity on the stability of a protein.

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7 January 2021

Cloning and sequence analysis of a cDNA encoding the beta-subunit of mouse beta-hexosaminidase

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https://api.crossref.org/works/10.1016%2FS0006-291X%2805%2981388-9

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7 January 2021

A point mutation in the coding sequence of the beta-hexosaminidase alpha gene results in defective processing of the enzyme protein in an unusual GM2-gangliosidosis variant

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https://api.crossref.org/works/10.1016%2FS0006-291X%2805%2981388-9

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7 January 2021

Activator proteins for lysosomal glycolipid hydrolysis

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retrieved

7 January 2021

Identifiers

DOI

10.1016/S0006-291X(05)81388-9

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PubMed ID

1720305

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(Q28281873)

Molecular basis of an adult form of beta-hexosaminidase B deficiency with motor neuron disease

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