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[HTML][HTML] Genomics of Wolfram Syndrome 1 (WFS1)

S Kõks - Biomolecules, 2023 - mdpi.com
Wolfram Syndrome (WFS) is a rare, autosomal, recessive neurogenetic disorder that affects
many organ systems. It is characterised by diabetes insipidus, diabetes mellites, optic …
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[HTML] nih.gov

[HTML][HTML] Genomics of Wolfram Syndrome 1 (WFS1)

S Kõks - Biomolecules, 2023 - ncbi.nlm.nih.gov
Wolfram Syndrome (WFS) is a rare, autosomal, recessive neurogenetic disorder that affects
many organ systems. It is characterised by diabetes insipidus, diabetes mellites, optic …

Genomics of Wolfram Syndrome 1 (WFS1)

S Kõks - Biomolecules, 2023 - agris.fao.org
Wolfram Syndrome (WFS) is a rare, autosomal, recessive neurogenetic disorder that affects
many organ systems. It is characterised by diabetes insipidus, diabetes mellites, optic …

Genomics of Wolfram Syndrome 1 (WFS1)

S Kõks - Biomolecules, 2023 - pubmed.ncbi.nlm.nih.gov
Wolfram Syndrome (WFS) is a rare, autosomal, recessive neurogenetic disorder that affects
many organ systems. It is characterised by diabetes insipidus, diabetes mellites, optic …

Genomics of Wolfram Syndrome 1 (WFS1)

S Kõks - Biomolecules, 2023 - search.proquest.com
Wolfram Syndrome (WFS) is a rare, autosomal, recessive neurogenetic disorder that affects
many organ systems. It is characterised by diabetes insipidus, diabetes mellites, optic …

Genomics of Wolfram Syndrome 1 (WFS1).

S Kõks - Biomolecules (2218-273X), 2023 - search.ebscohost.com
Wolfram Syndrome (WFS) is a rare, autosomal, recessive neurogenetic disorder that affects
many organ systems. It is characterised by diabetes insipidus, diabetes mellites, optic …

Genomics of Wolfram Syndrome 1 (WFS1)

S Kõks - Biomolecules, 2023 - europepmc.org
Wolfram Syndrome (WFS) is a rare, autosomal, recessive neurogenetic disorder that affects
many organ systems. It is characterised by diabetes insipidus, diabetes mellites, optic …
[PDF] murdoch.edu.au

[PDF][PDF] Genomics of Wolfram Syndrome 1 (WFS1). Biomolecules 2023, 13, 1346

S Kõks - 2023 - researchportal.murdoch.edu.au
Wolfram Syndrome (WFS) is a rare, autosomal, recessive neurogenetic disorder that affects
many organ systems. It is characterised by diabetes insipidus, diabetes mellites, optic …

Genomics of Wolfram Syndrome 1 (WFS1)

S Kõks - Biomolecules, 2023 - researchportal.murdoch.edu.au
Wolfram Syndrome (WFS) is a rare, autosomal, recessive neurogenetic disorder that affects
many organ systems. It is characterised by diabetes insipidus, diabetes mellites, optic …

Genomics of Wolfram Syndrome 1 (WFS1).

S Kõks - Biomolecules, 2023 - europepmc.org
Wolfram Syndrome (WFS) is a rare, autosomal, recessive neurogenetic disorder that affects
many organ systems. It is characterised by diabetes insipidus, diabetes mellites, optic …