[HTML][HTML] Molecular Features of SLC26A4 Common Variant p. L117F
A Matulevičius, E Bernardinelli, Z Brownstein… - Journal of Clinical …, 2022 - mdpi.com
The SLC26A4 gene, which encodes the anion exchanger pendrin, is involved in
determining syndromic (Pendred syndrome) and non-syndromic (DFNB4) autosomal …
determining syndromic (Pendred syndrome) and non-syndromic (DFNB4) autosomal …
Molecular Features of SLC26A4 Common Variant p. L117F.
A Matulevičius, E Bernardinelli… - Journal of Clinical …, 2022 - europepmc.org
The SLC26A4 gene, which encodes the anion exchanger pendrin, is involved in
determining syndromic (Pendred syndrome) and non-syndromic (DFNB4) autosomal …
determining syndromic (Pendred syndrome) and non-syndromic (DFNB4) autosomal …
Molecular Features of SLC26A4 Common Variant p. L117F.
A Matulevičius, E Bernardinelli… - Journal of Clinical …, 2022 - search.ebscohost.com
The SLC26A4 gene, which encodes the anion exchanger pendrin, is involved in
determining syndromic (Pendred syndrome) and non-syndromic (DFNB4) autosomal …
determining syndromic (Pendred syndrome) and non-syndromic (DFNB4) autosomal …
Molecular Features of SLC26A4 Common Variant p. L117F
A Matulevičius, E Bernardinelli… - Journal of clinical …, 2022 - pubmed.ncbi.nlm.nih.gov
The SLC26A4 gene, which encodes the anion exchanger pendrin, is involved in
determining syndromic (Pendred syndrome) and non-syndromic (DFNB4) autosomal …
determining syndromic (Pendred syndrome) and non-syndromic (DFNB4) autosomal …
[PDF][PDF] Molecular Features of SLC26A4 Common Variant p
A Matulevicius, E Bernardinelli, Z Brownstein… - L117F. J. Clin …, 2022 - researchgate.net
The SLC26A4 gene, which encodes the anion exchanger pendrin, is involved in
determining syndromic (Pendred syndrome) and non-syndromic (DFNB4) autosomal …
determining syndromic (Pendred syndrome) and non-syndromic (DFNB4) autosomal …
[HTML][HTML] Molecular Features of SLC26A4 Common Variant p. L117F
A Matulevičius, E Bernardinelli… - Journal of Clinical …, 2022 - ncbi.nlm.nih.gov
The SLC26A4 gene, which encodes the anion exchanger pendrin, is involved in
determining syndromic (Pendred syndrome) and non-syndromic (DFNB4) autosomal …
determining syndromic (Pendred syndrome) and non-syndromic (DFNB4) autosomal …
Molecular Features of SLC26A4 Common Variant p. L117F
A Matulevičius, E Bernardinelli… - Journal of Clinical …, 2022 - search.proquest.com
The SLC26A4 gene, which encodes the anion exchanger pendrin, is involved in
determining syndromic (Pendred syndrome) and non-syndromic (DFNB4) autosomal …
determining syndromic (Pendred syndrome) and non-syndromic (DFNB4) autosomal …
Molecular Features of SLC26A4 Common Variant p. L117F.
A Matulevičius, E Bernardinelli… - Journal of Clinical …, 2022 - europepmc.org
The SLC26A4 gene, which encodes the anion exchanger pendrin, is involved in
determining syndromic (Pendred syndrome) and non-syndromic (DFNB4) autosomal …
determining syndromic (Pendred syndrome) and non-syndromic (DFNB4) autosomal …