(Q43543967)

24 November 2017

Co-existence of lysosomal storage diseases in a consanguineous family (English)

1 reference

24 November 2017

Guy R

1

1 reference

24 November 2017

Forsyth JM

series ordinal

2

1 reference

24 November 2017

Cooper A

series ordinal

3

1 reference

24 November 2017

Morton RE

series ordinal

4

1 reference

24 November 2017

language of work or name

English

0 references

publication date

1 March 2001

1 reference

Child: Care, Health and Development

24 November 2017

1 reference

24 November 2017

27

1 reference

24 November 2017

2

1 reference

24 November 2017

173-181

1 reference

Follow-up in patients with aspartylglucosaminuria. Part I. The course of intellectual functions.

24 November 2017

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2214.2001.00165.X

Follow-up in patients with aspartylglucosaminuria. Part II. Adaptive skills.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2214.2001.00165.X

Human alpha-galactosidase A: nucleotide sequence of a cDNA clone encoding the mature enzyme

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2214.2001.00165.X

Molecular basis of Fabry disease: mutations and polymorphisms in the human alpha-galactosidase A gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2214.2001.00165.X

ABC of clinical genetics. Mendelian inheritance

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2214.2001.00165.X

10.1046/J.1365-2214.2001.00165.X

21 January 2018

Identifiers

DOI

1 reference

24 November 2017

1 reference