<p><a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0106656#pone.0106656-Stenson1" target="_blank">[50]</a> The mutations identified in OCA1 for each exon are described in the upper and lower half of the schema.</p
F each mutation within its exon, calculated as percentage of exon length. The lone spike around the ...
Some receptor tyrosine kinase genes are mutated in inherited and somatically acquired human cancers....
Tyrosine kinases (TKs) are central regulators of signaling pathways that control differentiation, tr...
<p>The novel mutations are marked by an asterisk. A: Exon structure of the <i>TYR</i> gene showing t...
<p>*The number in parenthesis in the status column shows the number of patients; New mutations are i...
Mutations in the Tyrosinase gene (TYR, 11q14–q21) cause oculocutaneous albinism type 1 (OCA1). The 3...
Item does not contain fulltextMutations in the Tyrosinase gene (TYR, 11q14-q21) cause oculocutaneous...
<p>Bar diagram indicates the percentage of mutations that were found in this study.</p
Oculocutaneous albinism (OCA) is a heterogeneous group of autosomal recessive disorders resulting fr...
Tyrosinase gene (TYR) encodes a protein that regulates the production of the pigment melanin, a prim...
PurposeTo investigate eight previously unreported Pakistani families with genetically undefined OCA ...
We analyzed the tyrosinase (TYR) gene of 12 Korean patients with various types of oculocutaneous alb...
<p>The top line shows a scale map of the region of the <i>Drosophila bithorax complex</i> from <i>ab...
Since the first report of a mutation in the tyrosinase gene that causes tyrosinase-negative oculocut...
is mutated in many cases of oculocutaneous albinism (OCA1), an autosomal recessive cause of childho...
F each mutation within its exon, calculated as percentage of exon length. The lone spike around the ...
Some receptor tyrosine kinase genes are mutated in inherited and somatically acquired human cancers....
Tyrosine kinases (TKs) are central regulators of signaling pathways that control differentiation, tr...
<p>The novel mutations are marked by an asterisk. A: Exon structure of the <i>TYR</i> gene showing t...
<p>*The number in parenthesis in the status column shows the number of patients; New mutations are i...
Mutations in the Tyrosinase gene (TYR, 11q14–q21) cause oculocutaneous albinism type 1 (OCA1). The 3...
Item does not contain fulltextMutations in the Tyrosinase gene (TYR, 11q14-q21) cause oculocutaneous...
<p>Bar diagram indicates the percentage of mutations that were found in this study.</p
Oculocutaneous albinism (OCA) is a heterogeneous group of autosomal recessive disorders resulting fr...
Tyrosinase gene (TYR) encodes a protein that regulates the production of the pigment melanin, a prim...
PurposeTo investigate eight previously unreported Pakistani families with genetically undefined OCA ...
We analyzed the tyrosinase (TYR) gene of 12 Korean patients with various types of oculocutaneous alb...
<p>The top line shows a scale map of the region of the <i>Drosophila bithorax complex</i> from <i>ab...
Since the first report of a mutation in the tyrosinase gene that causes tyrosinase-negative oculocut...
is mutated in many cases of oculocutaneous albinism (OCA1), an autosomal recessive cause of childho...
F each mutation within its exon, calculated as percentage of exon length. The lone spike around the ...
Some receptor tyrosine kinase genes are mutated in inherited and somatically acquired human cancers....
Tyrosine kinases (TKs) are central regulators of signaling pathways that control differentiation, tr...