Patel P. I., Franco В., Cook J. et al. Construction of a physical map on
mouse and human chromosome I: comparison of 13 Mb of mouse
and 11 Mb of human DNA//Hum. Mol. Genet. 1992. Vol.1. P. 613—
620.
Patel P. I., Roa В. В., Welcher A. A. et al. The gene for the peripheral
myelin protein PMP-22 is a candidate for Charcot-Marie-Tooth
disease type \NI Nature Genet. 1992a. Vol. 1. P. 159—165.
Pelin K., Hilpela P., Donner K. et al. Mutation in the nebulin gene
associated with autosomal recessive nemaline myopathy// Proc.
Nat. Acad Sci. 1999. Vol. 96. P. 2305—2310.
Peng H. В., Xie H., Rossi S. G., Rotundo R. L. Acetylcholinesterase
clustering at the neuromuscular junction involves perlecan and
dystroglycan//J. Cell Biol. 1999. Vol. 145. P. 911—921.
Pentao L, Wise C. A., Chinault A. C, Patel P. I., Lupski J. R. Charcot-
Marie-Tooth type IA duplication appears to arise from recombination
at repear sequences flanking the 1.5 Mb monomer unit// Nature
Genet. 1992. Vol. 2. P. 292—300.
Perrine S., Ginder G. D., Faller D. V. et al. A short-term trial of butyrate
to stimulate fetal-globin-gene expression in the beta-globin
disorders// New Engl. J. Med. 1993. Vol. 328. P. 81—86.
Piccolo F, Jeanpierre M., Leturcq F. et al. A founder mutation in the
gamma-sarcoglycan gene of Gypsies possibly predating their
migration out of India// Hum. Mol. Genet. 1996. Vol. 5. P. 2019—
2022.
Pham Y. C. N., thi Man N., Lam L. T, Morris G. E. Localization of myotonic
dystrophy protein kinase in human and rabbit tissues using a new
panel of monoclonal antibodies// Hum. Mol. Genet. 1998. Vol. 7.
P. 1957—1965.
Phillips W. D., Noakes P. G., Roberds S. L, Campbell K. P., Merlie J. P.
Clustering and immobilization of acetylcholine receptors by the 43kD
protein: a possible role for dystrophin-related protein// J. Cell Biol.
1993. Vol. 123. P. 729—740.
Piccolo F, Roberds S. L., Jeanpierre M. et al. Primary adhalinopathy: a
common cause of autosomal recessive muscular dystrophy of
variable severity// Nature Genet. 1995. Vol. 10. P. 243—245.
Pillers D.-A., Bulman D. E., Weleber R. G. et al. Dystrophin exprexion in
the human retina is required for normal function as defined by
electroretinography// Nature Genet. 1993. Vol. 4. P. 82—86.
288