Autosomal recessive cutis laxa syndrome revisited.
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(+info )Mutation in pyrroline-5-carboxylate reductase 1 gene in families with cutis laxa type 2.
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(+info )Fibulin 5 forms a compact dimer in physiological solutions.
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(+info )RIN2 deficiency results in macrocephaly, alopecia, cutis laxa, and scoliosis: MACS syndrome.
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(+info )Structural effects of fibulin 5 missense mutations associated with age-related macular degeneration and cutis laxa.
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(+info )Altered TGFbeta signaling and cardiovascular manifestations in patients with autosomal recessive cutis laxa type I caused by fibulin-4 deficiency.
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(+info )Ultrastructural demonstration of a relationship between acquired cutis laxa and monoclonal gammopathy.
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(+info )Mechanisms of emphysema in autosomal dominant cutis laxa.
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