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Fukuyama Type Congenital Muscular Dystrophy

Known as: WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, FKTN-RELATED, CMD, Fukuyama, muscular dystrophy fukuyama 
An autosomal recessive muscular dystrophy caused by mutations in the gene encoding fukutin (FKTN). It is associated with characteristic brain and eye… Expand
National Institutes of Health

Papers overview

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Highly Cited
2011
Highly Cited
2011
Fukuyama muscular dystrophy (FCMD; MIM253800), one of the most common autosomal recessive disorders in Japan, was the first human… Expand
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Highly Cited
2004
Highly Cited
2004
State-building—the creation of new governmental institutions and the strengthening of existing ones—is a crucial global issue… Expand
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Highly Cited
2003
Highly Cited
2003
The congenital muscular dystrophies (CMD) are a heterogeneous group of autosomal recessive disorders. A new pathomechanism has… Expand
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Highly Cited
2002
Highly Cited
2002
Fukuyama congenital muscular dystrophy (FCMD), muscle–eye–brain disease (MEB), and Walker–Warburg syndrome are congenital… Expand
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Highly Cited
2002
Highly Cited
2002
Muscle–eye–brain disease (MEB) and Fukuyama congenital muscular dystrophy (FCMD) are congenital muscular dystrophies with… Expand
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Highly Cited
2001
Highly Cited
2001
The congenital muscular dystrophies (CMD) are a heterogeneous group of autosomal recessive disorders presenting in infancy with… Expand
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Highly Cited
2001
Highly Cited
2001
BACKGROUND Fukuyama-type congenital muscular dystrophy (FCMD) is an autosomal recessive disorder characterized by severe… Expand
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Highly Cited
1999
Highly Cited
1999
Fukuyama-type congenital muscular dystrophy (FCMD), one of the most common autosomal recessive disorders in the Japanese… Expand
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Highly Cited
1998
Highly Cited
1998
Fukuyama-type congenital muscular dystrophy (FCMD), one of the most common autosomal recessive disorders in Japan (incidence is 0… Expand
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Highly Cited
1993
Highly Cited
1993
Fukuyama type congenital muscular dystrophy (FCMD) is an autosomal recessive severe muscular dystrophy associated with an anomaly… Expand
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