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Next generation sequencing identifies mutations in GNPTG gene as a cause of familial form of scleroderma-like disease
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نویسنده
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arowolo a.t. ,adeola h.a. ,khumalo n.p.
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منبع
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pediatric rheumatology - 2017 - دوره : 15 - شماره : 1
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چکیده
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[no abstract available]
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آدرس
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university of cape town,hair and skin research laboratory,division of dermatology,department of medicine,faculty of health sciences and groote schuur hospital,cape town, South Africa, university of cape town,hair and skin research laboratory,division of dermatology,department of medicine,faculty of health sciences and groote schuur hospital,cape town, South Africa, university of cape town,hair and skin research laboratory,division of dermatology,department of medicine,faculty of health sciences and groote schuur hospital,cape town, South Africa
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Authors
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