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Publications by S. K. Nissen

Identification of a Novel Mutation in the Factor VIII Gene Causing Severe Haemophilia A

Molecular Biology

English

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Psy139 - Current Use of Factor Viii Products in Children and Adolescents With Moderate or Severe Haemophilia A

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Factor XIa-triggered Thrombin Generation in Severe Haemophilia A

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A Novel Splice-Site Mutation in the GJB2 Gene Causing Mild Postlingual Hearing Impairment

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A Novel Mutation in the TG Gene (G2322S) Causing Congenital Hypothyroidism in a Sudanese Family: A Case Report

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A Novel Homozygous Mutation in the WNK1/HSN2 Gene Causing Hereditary Sensory Neuropathy Type 2.

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A Novel Missense Mutation p.L76P in the GJB2 Gene Causing Nonsyndromic Recessive Deafness in a Brazilian Family

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