Literature DB >> 17223882

Familial cutaneous collagenomas resulting from a novel mutation in LEMD3.

D Hershkovitz1, B Amitai, D B Amitai, E Sprecher.   

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Year:  2007        PMID： 17223882     DOI： 10.1111/j.1365-2133.2006.07651.x

Source DB:  PubMed          Journal:  Br J Dermatol        ISSN： 0007-0963            Impact factor:   9.302


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  4 in total

1.  A Report of a Novel Pathogenic Variant in a Family with Buschke-Ollendorf Syndrome.

Authors:  Angita Jain; Pavalan Selvam; Herjot Atwal; Paldeep S Atwal
Journal:  J Pediatr Genet       Date:  2019-08-26

2.  Reverse referral: from pathology to endocrinology.

Authors:  Selma Feldman Witchel; Sarangarajan Ranganathan; Megan Kilpatrick; Sally E Carty
Journal:  Endocr Pathol       Date:  2009       Impact factor: 3.943

3.  Novel 4-bp Intronic Deletion (c.1560+5_1560+8del) [corrected] in LEMD3 in a Korean Patient With Osteopoikilosis.

Authors:  In Young Yoo; Ju Sun Song; Chang Seok Ki; Jong Won Kim; Hoon Suk Cha; Yong Ki Min
Journal:  Ann Lab Med       Date:  2017-11       Impact factor: 3.464

4.  Mutation in LEMD3 (Man1) Associated with Osteopoikilosis and Late-Onset Generalized Morphea: A New Buschke-Ollendorf Syndrome Variant.

Authors:  Benjamin Korman; Jun Wei; Anne Laumann; Polly Ferguson; John Varga
Journal:  Case Rep Dermatol Med       Date:  2016-06-13
  4 in total

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