Could the ENPP1 p.D85H Mutation be Associated with Hypophosphatemic Rickets?
Objective:A 35-year-old Turkish male patient was referred to us with a year-long history of joint paint and congenital hearing loss. Family history revealed more family members with hearing loss without paraneoplastic syndrome. These findings led us to investigate the genetic alterations associated...
Main Authors: | Ender COŞKUNPINAR, Sakin TEKİN, Şükrü PALANDUZ, Hakan AVCI, Kıvanç CEFLE, N. Ozan TİRYAKİOĞLU, Ayşe KUBAT ÜZÜM, Refik TANAKOL, İlhan SATMAN |
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Format: | Article |
Language: | English |
Published: |
Galenos Publishing House
2018-04-01
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Series: | Bezmiâlem Science |
Subjects: | |
Online Access: |
http://bezmialemscience.org/archives/archive-detail/article-preview/could-the-enpp1-pd85h-mutation-be-associated-with-/20185
|
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