Schöpf‐Schulz‐Passarge syndrome associated with two new missense mutations in WNT10A

Publisher： John Wiley & Sons Inc

E-ISSN： 1610-0387|16|1|66-69

ISSN： 1610-0379

Source： JOURNAL DER DEUTSCHEN DERMATOLOGISCHEN GESELLSCHAFT, Vol.16, Iss.1, 2018-01, pp. : 66-69

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Related content

Syndromic parkinsonism and dementia associated with OPA1 missense mutations

By  

ANNALS OF NEUROLOGY, Vol. 78, Iss. 1, 2015-07 ,pp. : 21-38

John Wiley & Sons Inc

Access to resources Recommend Favorite

Severe scoliosis associated with the WNT10A mutation

By  

THE JOURNAL OF DERMATOLOGY, Vol. 42, Iss. 3, 2015-03 ,pp. : 322-323

John Wiley & Sons Inc

Access to resources Recommend Favorite

Identification of two novel missense mutations causing severe factor XIII deficiency

By  

HAEMOPHILIA, Vol. 21, Iss. 3, 2015-05 ,pp. : e253-e256

John Wiley & Sons Inc

Access to resources Recommend Favorite

Two novel Brugada syndrome-associated mutations increase KV4.3 membrane expression and function

By          

International Journal of Molecular Medicine, Vol. 36, Iss. 1, 2015-01 ,pp. : 309-315

Spandidos Publications

Access to resources Recommend Favorite

Two novel missense mutations of ATP2A2 in two Chinese patients with sporadic Darier Disease

By  

CLINICAL & EXPERIMENTAL DERMATOLOGY, Vol. 40, Iss. 2, 2015-03 ,pp. : 201-203

John Wiley & Sons Inc

Access to resources Recommend Favorite