Four novel mutations in the ALPL gene in Chinese patients with odonto, childhood, and adult hypophosphatasia

Παρόμοια τεκμήρια

• Clinical and genetic findings in a Chinese family with VDR-associated hereditary vitamin D-resistant rickets
  ανά: Pang, Qianqian, κ.ά.
  Έκδοση: (2016)
• The first case report of Kyphoscoliotic Ehlers-Danlos syndrome of chinese origin with a novel PLOD1 gene mutation
  ανά: Ni, Xiaolin, κ.ά.
  Έκδοση: (2020)
• The first case of primary hypertrophic osteoarthropathy with soft tissue giant tumors caused by HPGD loss-of-function mutation
  ανά: Qianqian Pang, κ.ά.
  Έκδοση: (2019-06-01)
• The first case of primary hypertrophic osteoarthropathy with soft tissue giant tumors caused by HPGD loss-of-function mutation
  ανά: Pang, Qianqian, κ.ά.
  Έκδοση: (2019)
• Two novel mutations in the ALPL gene of unrelated Chinese children with Hypophosphatasia: case reports and literature review
  ανά: Mao, Xiaojian, κ.ά.
  Έκδοση: (2019)