M. Chaouch

Primary adhalinopathy: a common cause of autosomal recessive muscular dystrophy of variable severity

Fédérica Piccolo, Steven L. Roberds, Marc Jeanpierre et al. · Nature Genetics · 1995 · 191 citations

Medicine, Neurology, Neuromuscular Disorders +3

Primary adhalinopathy (α‐sarcoglycanopathy)

B. Eymard, Norma B. Romero, France Leturcq et al. · Neurology · 1997 · 134 citations

Medicine, Genetics, Molecular Genetics +15

Severe childhood autosomal recessive muscular dystrophy with the deficiency of the 50 kDa dystrophin-associated glycoprotein maps to chromosome 13q12

Kemal Azlbi, L Bachner, J. Beckmann et al. · Human Molecular Genetics · 1993 · 101 citations

Life Sciences, Genetics, Molecular Genetics +9

The phenotypic manifestations of autosomal recessive axonalCharcot–Marie–Tooth due to a mutation in Lamin A/C gene

M. Chaouch, Y. Allal, Annachiara De Sandre‐Giovannoli et al. · Neuromuscular Disorders · 2002 · 90 citations

Life Sciences, Genetics, Molecular Genetics +3

Founder Effect and Estimation of the Age of the c.892C&gt;T (p.Arg298Cys) Mutation in <i>LMNA</i> Associated to Charcot‐Marie‐Tooth Subtype CMT2B1 in Families from North Western Africa

Tarik Hamadouche, Yannick Poitelon, Emmanuelle Génin et al. · Annals of Human Genetics · 2008 · 31 citations

Life Sciences, Genetics, Molecular Genetics +14