Protein Dysfunction in Human Genetic Disease

Buch | Hardcover

272 Seiten

1997
Bios Scientific Publishers Ltd (Verlag)
978-1-85996-036-3 (ISBN)

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Recent years have seen rapid advances in our understanding of genetic diseases in terms of their molecular origins. The book focuses on DNA mutations which give rise to abnormalities of protein structure and function in genetic disease.

Swallow/, DM; Edwards/, YH

Mutation and Protein Dysfunction; Haemoglobin: Glucose 6-phosphate Dehydrogenase; Glycogen Storage disease due to Phosphorylase Kinase Deficiency; The Retinoblastoma Tumour Suppressor Protein and Cancer; Rhodopsin Mutations in Photoreceptor Degeneration:

Erscheint lt. Verlag	15.6.1997
Verlagsort	London
Sprache	englisch
Maße	161 x 241 mm
Gewicht	635 g
Themenwelt	Medizin / Pharmazie ► Medizinische Fachgebiete
	Studium ► 2. Studienabschnitt (Klinik) ► Humangenetik
	Naturwissenschaften ► Biologie ► Biochemie
ISBN-10	1-85996-036-7 / 1859960367
ISBN-13	978-1-85996-036-3 / 9781859960363
Zustand	Neuware