aceruloplasminemia wikispaces.com

Aceruloplasminemia - home

Skip to main content. Create interactive lessons using any digital content including wikis with our free sister product TES Teach. Get it on the web. Acerulopasminemia was first discovered in 1987 by Miyajima. Et. Al it was first thought to be wilsons disease. Aceruloplasminemia is a -linked recessive disease. The gene affected was the CP gene. The gene provides instructions for making a protein called Ceraloplasmin that is involved in iron transport and processing in red blood cells.

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The domain aceruloplasminemia.wikispaces.com currently has an average traffic ranking of zero (the lower the higher page views). We have analyzed eleven pages within the domain aceruloplasminemia.wikispaces.com and found two websites interfacing with aceruloplasminemia.wikispaces.com. There is one public communication platforms linked to aceruloplasminemia.wikispaces.com.
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Aceruloplasminemia - home

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Skip to main content. Create interactive lessons using any digital content including wikis with our free sister product TES Teach. Get it on the web. Acerulopasminemia was first discovered in 1987 by Miyajima. Et. Al it was first thought to be wilsons disease. Aceruloplasminemia is a -linked recessive disease. The gene affected was the CP gene. The gene provides instructions for making a protein called Ceraloplasmin that is involved in iron transport and processing in red blood cells.

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The domain aceruloplasminemia.wikispaces.com has the following on the web site, "Create interactive lessons using any digital content including wikis with our free sister product TES Teach." I observed that the webpage also said " Get it on the web." They also stated " Acerulopasminemia was first discovered in 1987 by Miyajima. Al it was first thought to be wilsons disease. Aceruloplasminemia is a -linked recessive disease. The gene affected was the CP gene. The gene provides instructions for making a protein called Ceraloplasmin that is involved in iron transport and processing in red blood cells."

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Create interactive lessons using any digital content including wikis with our free sister product TES Teach. Get it on the web. Cogenital generalized hypertrichosis is a rare disorder which is noticed by excessive hair growth on the face and upper-body. The discovery of a mexican family with the disorder helped scientists the chance to track the gene. Dr Pragana Patel identified the gene. It is an X-linked dominant pattern of inheritance.

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