The pallid gene encodes a novel, syntaxin 13-interacting protein involved in platelet storage pool deficiency

Author:

Huang Liping,Kuo Yien-Ming,Gitschier Jane

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Reference28 articles.

1. Roberts, E. A new mutation in the house mouse (Mus musculus). Science 74, 569 (1931).

2. Novak, E.K., Hui, S.-W. & Swank, R.T. Platelet storage pool deficiency in mouse pigment mutations associated with seven distinct genetic loci. Blood 63, 536–544 (1984).

3. Lyon, M.F. & Searle, A.G. Genetic Variants and Strains of the Laboratory Mouse 274–275, 841 (Oxford University Press, Oxford, 1989).

4. Martorana, P.A. et al. The pallid mouse. A model of genetic α1-antitrypsin deficiency. Lab. Invest. 68, 233–241 (1993).

5. Theriault, L.L. & Hurley, L.S. Ultrastructure of developing melanosomes in C57 black and pallid mice. Dev. Biol. 23, 261–275 (1970).

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