Literature DB >> 23312576

MC1R gene mutation and its association with oculocutaneous albinism type (OCA) phenotype in a consanguineous Pakistani family.

Shamim B Saleha, Muhammad Ajaml, Muhammad Jamil, Muhammad Nasir, Abdul Hameed.   

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Year:  2012        PMID： 23312576     DOI： 10.1016/j.jdermsci.2012.11.591

Source DB:  PubMed          Journal:  J Dermatol Sci        ISSN： 0923-1811            Impact factor:   4.563


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  2 in total

Review 1.  MC1R, the cAMP pathway, and the response to solar UV: extending the horizon beyond pigmentation.

Authors:  Jose C García-Borrón; Zalfa Abdel-Malek; Celia Jiménez-Cervantes
Journal:  Pigment Cell Melanoma Res       Date:  2014-05-30       Impact factor: 4.693

Review 2.  Oculocutaneous Albinism and Squamous Cell Carcinoma of the Skin of the Head and Neck in Sub-Saharan Africa.

Authors:  P T Lekalakala; R A G Khammissa; B Kramer; O A Ayo-Yusuf; J Lemmer; L Feller
Journal:  J Skin Cancer       Date:  2015-08-12
  2 in total

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