Scholars@Duke publication: X-linked myopathy with excessive autophagy (XMEA): clinical spectrum, refined mapping and mutation screening.

X-linked myopathy with excessive autophagy (XMEA): clinical spectrum, refined mapping and mutation screening.

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Alic, SA; Aiyar, R; Juel, V; Mandell, J; Villanova, M; Fardeau, M; Scherer, SW; Auranen, M; Kalimo, H; Minassian, BA

Published in: AMERICAN JOURNAL OF HUMAN GENETICS

2001

AMERICAN JOURNAL OF HUMAN GENETICS

0002-9297

2001

538 / 538

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Alic, S. A., Aiyar, R., Juel, V., Mandell, J., Villanova, M., Fardeau, M., … Minassian, B. A. (2001). X-linked myopathy with excessive autophagy (XMEA): clinical spectrum, refined mapping and mutation screening. In AMERICAN JOURNAL OF HUMAN GENETICS (Vol. 69, pp. 538–538).

Alic, S. A., R. Aiyar, V. Juel, J. Mandell, M. Villanova, M. Fardeau, S. W. Scherer, M. Auranen, H. Kalimo, and B. A. Minassian. “X-linked myopathy with excessive autophagy (XMEA): clinical spectrum, refined mapping and mutation screening.” In AMERICAN JOURNAL OF HUMAN GENETICS, 69:538–538, 2001.

Alic SA, Aiyar R, Juel V, Mandell J, Villanova M, Fardeau M, et al. X-linked myopathy with excessive autophagy (XMEA): clinical spectrum, refined mapping and mutation screening. In: AMERICAN JOURNAL OF HUMAN GENETICS. 2001. p. 538–538.

Alic SA, Aiyar R, Juel V, Mandell J, Villanova M, Fardeau M, Scherer SW, Auranen M, Kalimo H, Minassian BA. X-linked myopathy with excessive autophagy (XMEA): clinical spectrum, refined mapping and mutation screening. AMERICAN JOURNAL OF HUMAN GENETICS. 2001. p. 538–538.

AMERICAN JOURNAL OF HUMAN GENETICS

0002-9297

2001

538 / 538