Genetic and physical mapping of the Chediak-Higashi syndrome on chromosome 1q42-43.

The Chediak-Higashi syndrome (CHS) is a severe autosomal recessive condition, features of which are partial oculocutaneous albinism, increased susceptibility to infections, deficient natural killer cell activity, and the presence of large intracytoplasmic granulations in various cell types. Similar...

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Hlavní autoři: Barrat, F. J., Auloge, L., Pastural, E., Lagelouse, R. D., Vilmer, E., Cant, A. J., Weissenbach, J., Le Paslier, D., Fischer, A., de Saint Basile, G.
Médium: Artigo
Jazyk:Inglês
Vydáno: 1996
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Research Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC1914920/
https://ncbi.nlm.nih.gov/pubmed/8751864
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