Identification of a locus for an autosomal recessive hyaline body myopathy at chromosome 3p22.2-p21.32

By Onengut S.   Ugur S.A.   Karasoy H.   Yuceyar N.   Tolun A.  

Neuromuscular Disorders, Vol. 14, Iss. 1, 2004-01 ,pp. : 4-9

Elsevier

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A novel autosomal dominant spinocerebellar ataxia (SCA22) linked to chromosome 1p21-q23

By Chung M-y.  

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Oxford University Press

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A novel Twinkle gene mutation in autosomal dominant progressive external ophthalmoplegia

By Deschauer M.   Kiefer R.   Blakely E.L.   He L.   Zierz S.   Turnbull D.M.   Taylor R.W.  

Neuromuscular Disorders, Vol. 13, Iss. 7, 2003-09 ,pp. : 568-572

Elsevier

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Autosomal dominant hereditary spastic paraparesis with cognitive loss linked to chromosome 2p

By Webb S   Coleman D   Byrne P   Parfrey N   Burke T   Hutchinson J   Hutchinson M  

Brain, Vol. 121, Iss. 4, 1998-04 ,pp. : 601-609

Oxford University Press

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Leucodysplasia, microcephaly, cerebral malformation (LMC): a novel recessive disorder linked to 2p16

By Chandler K. E.   Del Rio A.   Rakshi K.   Springell K.   Williams D. K.   Stoodley N.   Woods C. G.   Pilz D. T.  

Brain, Vol. 129, Iss. 1, 2006-01 ,pp. : 272-277

Oxford University Press

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