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Discriminative Features in Three Autosomal Recessive Cutis Laxa Syndromes: Cutis Laxa IIA, Cutis Laxa IIB, and Geroderma Osteoplastica

Cutis laxa is a heterogeneous condition characterized by redundant, sagging, inelastic, and wrinkled skin. The inherited forms of this disease are rare and can have autosomal dominant, autosomal recessive, or X-linked inheritance. Three of the autosomal recessive cutis laxa syndromes, namely cutis l...

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Αποθηκεύτηκε σε:
Λεπτομέρειες βιβλιογραφικής εγγραφής
Τόπος έκδοσης:Int J Mol Sci
Κύριοι συγγραφείς: Kariminejad, Ariana, Afroozan, Fariba, Bozorgmehr, Bita, Ghanadan, Alireza, Akbaroghli, Susan, Khorram Khorshid, Hamid Reza, Mojahedi, Faezeh, Setoodeh, Aria, Loh, Abigail, Tan, Yu Xuan, Escande-Beillard, Nathalie, Malfait, Fransiska, Reversade, Bruno, Gardeitchik, Thatjana, Morava, Eva
Μορφή: Artigo
Γλώσσα:Inglês
Έκδοση: MDPI 2017
Θέματα:
Διαθέσιμο Online:https://ncbi.nlm.nih.gov/pmc/articles/PMC5372648/
https://ncbi.nlm.nih.gov/pubmed/28294978
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijms18030635
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