Scholars@Duke publication: Asymptomatic patient with myophosphorylase deficiency, high CK, and the L396P mutation

Asymptomatic patient with myophosphorylase deficiency, high CK, and the L396P mutation

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Gospe, SM; ElSchahawi, M; Shanske, S; Bruno, C; DiMauro, S; Hoye, E; Walsh, DA; Gorin, FA

Published in: NEUROLOGY

March 1, 1997

NEUROLOGY

0028-3878

March 1, 1997

5113 / 5113

LIPPINCOTT-RAVEN PUBL

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Chicago

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Gospe, S. M., ElSchahawi, M., Shanske, S., Bruno, C., DiMauro, S., Hoye, E., … Gorin, F. A. (1997). Asymptomatic patient with myophosphorylase deficiency, high CK, and the L396P mutation. In NEUROLOGY (Vol. 48, pp. 5113–5113). LIPPINCOTT-RAVEN PUBL.

Gospe, S. M., M. ElSchahawi, S. Shanske, C. Bruno, S. DiMauro, E. Hoye, D. A. Walsh, and F. A. Gorin. “Asymptomatic patient with myophosphorylase deficiency, high CK, and the L396P mutation.” In NEUROLOGY, 48:5113–5113. LIPPINCOTT-RAVEN PUBL, 1997.

Gospe SM, ElSchahawi M, Shanske S, Bruno C, DiMauro S, Hoye E, et al. Asymptomatic patient with myophosphorylase deficiency, high CK, and the L396P mutation. In: NEUROLOGY. LIPPINCOTT-RAVEN PUBL; 1997. p. 5113–5113.

Gospe, S. M., et al. “Asymptomatic patient with myophosphorylase deficiency, high CK, and the L396P mutation.” NEUROLOGY, vol. 48, no. 3, LIPPINCOTT-RAVEN PUBL, 1997, pp. 5113–5113.

Gospe SM, ElSchahawi M, Shanske S, Bruno C, DiMauro S, Hoye E, Walsh DA, Gorin FA. Asymptomatic patient with myophosphorylase deficiency, high CK, and the L396P mutation. NEUROLOGY. LIPPINCOTT-RAVEN PUBL; 1997. p. 5113–5113.

NEUROLOGY

0028-3878

March 1, 1997

5113 / 5113

LIPPINCOTT-RAVEN PUBL