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

Authors :: Alic, S.A.
Aiyar, R.
Juel, V.
Mandell, J.
Villanova, M.
Fardeau, M.
Scherer, S.W.
Auranen, M.
Kalimo, H.
Minassian, B.A.
Source :: American Journal of Human Genetics. Oct, 2001, Vol. 69 Issue 4, 538
Publication Year :: 2001

Subjects :: Human genetics -- Research
Genetic disorders -- Research
Cardiomyopathy -- Genetic aspects
Mental retardation -- Genetic aspects
Biological sciences

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