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Novel mutation in Patients with Microcephalic Osteodysplastic Primordial Dwarfism Type II (MOPD II)

2024-07-19

Abstract excerpt

<title>Abstract</title> <p>Background A rare type of autosomal recessive skeletal disorder known as microcephalic osteodysplastic primordial dwarfism (MOPD) type II causes a wide range of clinical abnormalities, including skeletal dysplasia, microcephaly, abnormal skin pigmentation, Insulin resistance, typical facial features and severe tooth deformities. Owing to the diverse nature of MOPD disorders and common...

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Literature Corpus work
9fabab4f-3e87-5627-b351-fc36ef9e612f
DOI
10.21203/rs.3.rs-4584884/v1
Open publication

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Novel mutation in Patients with Microcephalic Osteodysplastic Primordial Dwarfism Type II (MOPD II)DOI 10.21203/rs.3.rs-4584884/v1
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